Resources Contact Us Home Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE     Imidazolesulfonamide derivatives and herbicides 4830660 Imidazolesulfonamide derivatives and herbicides Patent Drawings: Inventor: Yamamoto, et al. Date Issued: May 16, 1989 Application: 07/059,608 Filed: June 8, 1987 Inventors: Hattori; Kenji (Shiraoka, JP) Ikai; Takashi (Shiraoka, JP) Kakuta; Takuya (Funabashi, JP) Morimoto; Katsushi (Funabashi, JP) Nawamaki; Tsutomu (Shiraoka, JP) Oya; Eiichi (Funabashi, JP) Sato; Toshiaki (Funabashi, JP) Yamamoto; Susumu (Funabashi, JP) Assignee: Nissan Chemical Industries, Ltd. (Tokyo, JP) Primary Examiner: Ford; John M. Assistant Examiner: Attorney Or Agent: Frishauf, Holtz, Goodman & Woodward U.S. Class: 504/178; 504/181; 504/211; 504/213; 504/215; 504/229; 504/230; 504/236; 504/237; 504/238; 504/239; 504/242; 504/243; 504/250; 504/253; 504/262; 504/263; 504/264; 504/265; 504/266; 504/269; 504/270; 504/271; 504/273; 544/182; 544/212; 544/278; 544/295; 544/296; 544/316; 544/317; 544/319; 544/320; 544/321; 544/324; 544/327; 544/328; 544/331 Field Of Search: 71/92; 71/90; 544/212; 544/182; 544/295; 544/296; 544/320; 544/321; 544/324; 544/331; 544/278; 544/316; 544/317; 544/319; 544/327; 544/328 International Class: U.S Patent Documents: Foreign Patent Documents: 0095925; 0096003; 58-162587; 60-45572 Other References: Abstract: There is disclosed imidazolesulfonamide derivatives represented by the general formula (I): ##STR1## wherein Q, m, R, B, D and T represent a group as specified in the specification andherbicides containing the same as an active ingredient. Claim: We claim: 1. An imidazolesulfonamide derivative represented by the formula (I): ##STR38## wherein Q represents a group of: ##STR39## wherein R.sup.1, R.sup.2 and R.sup.3 each independentlyrepresent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a halogenated lower alkyl group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a group of NR.sup.12 R.sup.13, a lower alkoxy group, a group ofSO.sub.2 NR.sup.8 R.sup.9, a group of SO.sub.2 OR.sup.11 or a phenyl group which may be substituted by a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.4 and R.sup.5 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated lower alkyl group, a nitro group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a lower alkoxy group ora phenyl group which may be substituted by a halogen atom, a group of COOR.sup.10, a nitro group, a lower alkoxy group or a lower alkyl group; R.sup.6 and R.sup.7 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a group of COOR.sup.10 ; R.sup.8 and R.sup.9 each independently represent a hydrogen atom, a lower alkyl group or a phenyl group; W.sup.1 represents an oxygen atom, a sulfur atom or a group of N--R.sup.10 ; R.sup.10 represents a hydrogen atom or a lower alkyl group; R.sup.11 represents a lower alkyl group and n represents an integer of 0, 1 or 2; and R.sup.12 and R.sup.13 each independently represent a hydrogen atom or a lower alkyl group; m represents an integer of 0, 1 or 2; R represents a hydrogen atom or a lower alkyl group; B and D each independently represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a lower aralkyl group, a lower alkoxy group, a halogenated lower alkyl group, a halogenated lower alkenyl group, a lower alkoxyalkyl group,an alkylcarbonyl group, a group of COOR.sup.14, a group of CONR.sup.15 R.sup.16, a group of S(O).sub.n R.sup.17, a cyano group, a group of NR.sup.18 R.sup.19, a group of SO.sub.2 NR.sup.20 R.sup.21, a group of OH, a benzoyl group which may be substitutedby a halogen atom or a lower alkyl group or a phenyl group which may substituted by is selected from a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.14 represents a hydrogen atom, a lower alkyl group which may be substituted by a group of OR.sup.10, a halogen atom, a halogenated lower alkoxy group, a cyano group, a phenoxy group, a lower alkoxycarbonyl group, a group of NR.sup.10R.sup.11, a lower cycloalkyl group, a lower alkylthio group or a lower alkylcarbonyl group, a lower alkenyl group, a halogenated lower alkenyl group, a lower alkynyl group, a halogenated lower alkynyl group, a lower cycloalkyl group or a benzyl group; R.sup.15 represents a hydrogen atom, a lower alkyl group or a phenyl group; and R.sup.16 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.17 represents a lower alkyl group, a lower alkoxy group, a phenyl group, a halogenated alkyl group, a lower alkenyloxy group or a lower alkynyloxy group; and n represents an integer of 0, 1 or 2; R.sup.18 and R.sup.19 each independently represent a hydrogen atom, a lower alkyl group, a lower alkylcarbonyl group or a lower alkylsulfonyl group; R.sup.20 and R.sup.21 each independently represent a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; T represents a group of ##STR40## E represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower alkoxy group; G represents a group of; ##STR41## wherein X and Y each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkoxyalkyl group, a halogenated alkyl group, a halogenated lower alkoxy group, agroup of NR.sup.24 R.sup.25, a group of OCH(R.sup.10)--COOR.sup.10, a group of COOR.sup.10, a cyclopropyl group, a group of CH(OR.sup.26).sub.2, a lower alkylthio group or a halogenated lower alkylthio group; R.sup.24 and R.sup.25 each independently represent a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.26 represents a lower alkyl group; X.sup.1 and Y.sup.1 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated alkyl group or a lower alkoxy group; Z represents a group of C--R.sup.27 ; H.sup.27 represents a hydrogen atom, a lower alkyl group, a halogenated lower alkyl group, a halogen atom, a lower alkoxy group or a 5-membered ring structure containing an oxygen atom together with Y or Y.sup.1 ; W represents an oxygen atom, a sulfur atom or a group of N--R.sup.28 where R.sup.28 represents a hydrogen atom or a lower alkoxy group; W.sup.2 represents an oxygen atom or a sulfur atom; R.sup.22 represents a lower alkyl group; Az represents a halogen atom, a nitro group, or an imidazolyl group, an imidazolynyl group, a pyrazolyl group, a triazolyl group or a benzimidazolyl group each of which may be mono-, di- or tri-substituted by a lower alkyl group; J represents a lower alkyl group or a group of; ##STR42## wherein Q, R, m, B and D have the same meanings as defined above; R.sup.23 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group. 2. The compound of claim 1, which is represented by the formula: ##STR43## wherein R.sub.1 represents a hydrogen atom, a methyl group or a halogen atom; R represents a methyl group or an ethyl group; Q is selected from the group of Q5, Q6, Q7,Q9, Q15, Q21, Q26, Q29, Q32, Q50, Q54, Q61, Q68, Q88, Q127, Q138, Q142, Q188, Q189, Q201, Q202, Q204, Q205, Q209, Q222, Q225, Q229, Q230, Q246 and Q250 as shown below: ##STR44## X and Y are each independently a halogen atom, a methyl group, a methoxygroup; and Z is --CH.dbd.. 3. The compound of claim 2, which is N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-ethoxycarbonyl-1-(2-thiaz olyl)imidazole-5-sulfonamide. 4. The compound of claim 2, which is N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-methoxycarbonyl-1-(2-thia zolyl)imidazole-5-sulfonamide. 5. The compound of claim 2, which is N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-methoxycarbonyl-1-(1,3,4- thiadiazol-2-yl)imidazole-5-sulfonamide. 6. The compound of claim 2, which is N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-4-methoxycarbonyl-1-(2-pyrid yl)imidazole-5-sulfonamide. 7. The compound of claim 2, which is N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-methoxycarbonyl-1-(2-pyri midyl)imidazole-5-sulfonamide. 8. The compound of claim 1, which is represented by the formula: ##STR45## wherein R.sub.1 represents a hydrogen atom or a methyl group; R represents a methyl group or an ethyl group; Q is selected from the group of Q5, Q6, Q7, Q9, Q15, Q21,Q26, Q29, Q32, Q50, Q54, Q61, Q68, Q88, Q127, Q138, Q142, Q188, Q189, Q201, Q202, Q204, Q205, Q209, Q222, Q225, Q229, Q230, Q246 and Q250 as shown below: ##STR46## X and Y are each independently a halogen atom, a methyl group, a methoxy group; and Z is--CH.dbd.. 9. The compound of claim 1, which is represented by the formula: ##STR47## wherein R.sub.1 represents a hydrogen atom, a methyl group, a halogen atom or a nitro group; R represents a methyl group or an ethyl group; Q is selected from the groupof Q5, Q6, Q7, Q9, Q15, Q21, Q26, Q29, Q32, Q50, Q54, Q61, Q68, Q88, Q127, Q138, Q142, Q188, Q189, Q201, Q202, Q204, Q205, Q209, Q222, Q225, Q229, Q230, Q246 and Q250 as shown below: ##STR48## X and Y are each independently a halogen atom, a methylgroup, a methoxy group; and Z is --CH.dbd.. 10. The compound of claim 2, which is N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-ethoxycarbonyl-1-(2-pyrid yl)imidazole-5-sulfonamide. 11. The compound of claim 2, which is the compound where R is an ethyl group, R.sub.1 is a hydrogen atom and Q is Q204. 12. The compound of claim 11, wherein X and Y are each independently selected from methyl and methoxy. 13. The compound of claim 12, wherein X and Y are each methoxy. 14. The compound of claim 2, which is the compound where R is an ethyl group, R.sub.1 is a hydrogen atom and Q is Q222. 15. The compound of claim 14, wherein X and Y are each independently selected from methyl and methoxy. 16. The compound of claim 15, wherein X and Y are each methoxy. 17. The compound of claim 1, wherein G is ##STR49## 18. A method for inhibiting growth of undesirable plants by using the compound represented by the formula (I): ##STR50## wherein Q represents a group of: ##STR51## wherein R.sup.1, R.sup.2 and R.sup.3 each independently represent a hydrogenatom, a halogen atom, a nitro group, a lower alkyl group, a halogenated lower alkyl group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a group of NR.sup.12 R.sup.13, a lower alkoxy group, a group of SO.sub.2 NR.sup.8 R.sup.9, a group of SO.sub.2 OR.sup.11 or a phenyl group which may be substituted by ahalogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.4 and R.sup.5 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated lower alkyl group, a nitro group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a lower alkoxy group ora phenyl group which may be substituted by a halogen atom, a group of COOR.sup.10, a nitro group, a lower alkoxy group or a lower alkyl group; R.sup.6 and R.sup.7 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a group of COOR.sup.10 ; R.sup.8 and R.sup.9 each independently represent a hydrogen atom, a lower alkyl group or a phenyl group; W.sup.1 represents an oxygen atom, a sulfur atom or a group of N--R.sup.10 ; R.sup.10 represents a hydrogen atom or a lower alkyl group; R.sup.11 represents a lower alkyl group and n represents an integer of 0, 1 or 2; and R.sup.12 and R.sup.13 each independently represent a hydrogen atom or a lower alkyl group; m represents an integer of 0, 1 or 2; R represents a hydrogen atom or a lower alkyl group; B and D each independently represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a lower aralkyl group, a lower alkoxy group, a halogenated lower alkyl group, a halogenated lower alkenyl group, a lower alkoxyalkyl group,an alkylcarbonyl group, a group of COOR.sup.14, a group of CONR.sup.15 R.sup.16, a group of S(O).sub.n R.sup.17, a cyano group, a group of NR.sup.18 R.sup.19, a group of SO.sub.2 NR.sup.20 R.sup.21, a group of OH, a benzoyl group which may be substitutedby a halogen atom or a lower alkyl group or a phenyl group which may substituted by is selected from a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.14 represents a hydrogen atom, a lower alkyl group which may be substituted by a group of OR.sup.10, a halogen atom, a halogenated lower alkoxy group, a cyano group, a phenoxy group, a lower alkoxycarbonyl group, a group of NR.sup.10R.sup.11, a lower cycloalkyl group, a lower alkylthio group or a lower alkylcarbonyl group, a lower alkenyl group, a halogenated lower alkenyl group, a lower alkynyl group, a halogenated lower alkynyl group, a lower cycloalkyl group or a benzyl group; R.sup.15 represents a hydrogen atom, a lower alkyl group or a phenyl group; and R.sup.16 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.17 represents a lower alkyl group, a lower alkoxy group, a phenyl group, a halogenated alkyl group, a lower alkenyloxy group or a lower alkynyloxy group; and n represents an integer of 0, 1 or 2; R.sup.18 and R.sup.19 each independently represent a hydrogen atom, a lower alkyl group, a lower alkylcarbonyl group or a lower alkylsulfonyl group; R.sup.20 and R.sup.21 each independently represent a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; T represents a group of ##STR52## E represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower alkoxy group; G represents a group of: ##STR53## wherein X and Y each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkoxyalkyl group, a halogenated alkyl group, a halogenated lower alkoxy group, agroup of NR.sup.24 R.sup.25, a group of OCH(R.sup.10)--COOR.sup.10, a group of COOR.sup.10, a cyclopropyl group, a group of CH(OR.sup.26).sub.2, a lower alkylthio group or a halogenated lower alkylthio group; R.sup.24 and R.sup.25 each independently represent a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.26 represents a lower alkyl group; X.sup.1 and Y.sup.1 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group; a halogenated alkyl group or a lower alkoxy group; Z represents a group of C--R.sup.27 ; R.sup.27 represents a hydrogen atom, a lower alkyl group, a halogenated lower alkyl group, a halogen atom, a lower alkoxy group or a 5-membered ring structure containing an oxygen atom together with Y or Y.sup.1 ; W represents an oxygen atom, a sulfur atom or a group of N--R.sup.28 where R.sup.28 represents a hydrogen atom or a lower alkoxy group; W.sup.2 represents an oxygen atom or a sulfur atom; R.sup.22 represents a lower alkyl group; Az represents a halogen atom, a nitro group, or an imidazolyl group, an imidazolynyl group, a pyrazolyl group, a triazolyl group or a benzimidazolyl group each of which may be mono-, di- or tri-substituted by a lower alkyl group; J represents a lower alkyl group or a group of; ##STR54## wherein Q, R, m, B and D have the same meanings as defined above; R.sup.23 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group. 19. The method of claim 18, wherein G is ##STR55## 20. A herbicide which comprises a herbicidal carrier and as an effective ingredient, a compound represented by the formula (I): ##STR56## wherein Q represents a group of; ##STR57## wherein R.sup.1, R.sup.2 and R.sup.3 each independentlyrepresent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a halogenated lower alkyl group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a group of NR.sup.12 R.sup.13, a lower alkoxy group, a group ofSO.sub.2 NR.sup.8 R.sup.9, a group of SO.sub.2 OR.sup.11 or a phenyl group which may be substituted by a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.4 and R.sup.5 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated lower alkyl group, a nitro group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a lower alkoxy group ora phenyl group which may be substituted by a halogen atom, a group of COOR.sup.10, a nitro group, a lower alkoxy group or a lower alkyl group; R.sup.6 and R.sup.7 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a group of COOR.sup.10 ; R.sup.8 and R.sup.9 each independently represent a hydrogen atom, a lower alkyl group or a phenyl group; W.sup.1 represents an oxygen atom, a sulfur atom or a group of N--R.sup.10 ; R.sup.10 represents a hydrogen atom or a lower alkyl group; R.sup.11 represents a lower alkyl group and n represents an integer of 0, 1 or 2; and R.sup.12 and R.sup.13 each independently represent a hydrogen atom or a lower alkyl group; m represents an integer of 0, 1 or 2; R represents a hydrogen atom or a lower alkyl group; B and D each independently represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a lower aralkyl group, a lower alkoxy group, a halogenated lower alkyl group, a halogenated lower alkenyl group, a lower alkoxyalkyl group,an alkylcarbonyl group, a group of COOR.sup.14, a group of CONR.sup.15 R.sup.16, a group of S(O).sub.n R.sup.17, a cyano group, a group of NR.sup.18 R.sup.19, a group of SO.sub.2 NR.sup.20 R.sup.21, a group of OH, a benzoyl group which may be substitutedby a halogen atom or a lower alkyl group or a phenyl group which may substituted by is selected from a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group or a lower alkyl group; R.sup.14 represents a hydrogen atom, a lower alkyl group which may be substituted by a group of OR.sup.10, a halogen atom, a halogenated lower alkoxy group, a cyano group, a phenoxy group, a lower alkoxycarbonyl group, a group of NR.sup.10R.sup.11, a lower cycloalkyl group, a lower alkylthio group or a lower alkylcarbonyl group, a lower alkenyl group, a halogenated lower alkenyl group, a lower alkynyl group, a halogenated lower alkynyl group, a lower cycloalkyl group or a benzyl group; R.sup.15 represents a hydrogen atom, a lower alkyl group or a phenyl group; and R.sup.16 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.17 represents a lower alkyl group, a lower alkoxy group, a phenyl group, a halogenated alkyl group, a lower alkenyloxy group or a lower alkynyloxy group; and n represents an integer of 0, 1 or 2; R.sup.18 and R.sup.19 each independently represent a hydrogen atom, a lower alkyl group, a lower alkylcarbonyl group or a lower alkylsulfonyl group; R.sup.20 and R.sup.21 each independently represent a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; T represents a group of ##STR58## E represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower alkoxy group; G represents a group of; ##STR59## wherein X and Y each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkoxyalkyl group, a halogenated alkyl group, a halogenated lower alkoxy group, agroup of NR.sup.24 R.sup.25, a group of OCH(R.sup.10)--COOR.sup.10, a group of COOR.sup.10, a cyclopropyl group, a group of CH(OR.sup.26).sub.2, a lower alkylthio group or a halogenated lower alkylthio group; R.sup.24 and R.sup.25 each independently represent a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.26 represents a lower alkyl group; X.sup.1 and Y.sup.1 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated alkyl group or a lower alkoxy group; Z represents a group of C--R.sup.27 ; R.sup.27 represents a hydrogen atom, a lower alkyl group, a halogenated lower alkyl group, a halogen atom, a lower alkoxy group or a 5-membered ring structure containing an oxygen atom together with Y or Y.sup.1 ; W represents an oxygen atom, a sulfur atom or a group of N--R.sup.28 where R.sup.28 represents a hydrogen atom or a lower alkoxy group; W.sup.2 represents an oxygen atom or a sulfur atom; R.sup.22 represents a lower alkyl group; Az represents a halogen atom, a nitro group, or an imidazolyl group, an imidazolynyl group, a pyrazolyl group, a triazolyl group or a benzimidazolyl group each of which may be mono-, di- or tri-substituted by a lower alkyl group; J represents a lower alkyl group or a group of; ##STR60## wherein Q, R, m, B and D have the same meanings as defined above; R.sup.23 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group. 21. The herbicide of claim 20, wherein G is ##STR61## Description: BACKGROUND OF THE INVENTION This invention relates to a novel imidazolesulfonamide derivative, a process for preparing the compound and a herbicide containing the compound as an active ingredient. In order to protect important crops such as rice plants, wheat, corn, soybean, cotton, beat, etc. from damages by weeds to achieve an increased yield, it is indispensable to use a herbicide. In recent years in particular, a herbicide havingselectivity (or discriminativity) is sought after as it can kill only weeds selectively without damages to crops even when a foliage treatment with the herbicide is applied simultaneously on crops and weeds in a cultivated land wherein useful crops andweeds are grown together. Also, from viewpoints of prevention of environmental pollution, the transportation, and the economical cost reduction in application of chemicals, studies and researches have been made over many years on such compounds that mayachieve a higher herbicidal activity with use of chemicals in a lower amount. Some of the compounds having such a property are presently used as the herbicide having selectivity. Still, however, there are further demands for new compounds having such aproperty. SUMMARY OF THE INVENTION The present inventors have made researches over many years to develop herbicides having the selectivity on important crops, and have examined herbicidal properties of a number of compounds to create compounds having a higher herbicidal effect andthe selectivity. As a result, it was found that an imidazolesulfonamide derivative represented by general Formula (I) (hereinafter referred to as "the compound of this invention): ##STR2## wherein Q represents a group of; ##STR3## wherein R.sup.1,R.sup.2 and R.sup.3 each independently represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, a halogenated lower alkyl group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a group of NR.sup.12 R.sup.13, alower alkoxy group, a group of SO.sub.2 NR.sup.8 R.sup.9, a group of SO.sub.2 OR.sup.11 or a phenyl group which may be substituted (the substituent is selected from a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group and a loweralkyl group); R.sup.4 and R.sup.5 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated loweralkyl group, a nitro group, a cyano group, a group of COOR.sup.10, a group of S(O).sub.n R.sup.11, a lower alkoxy group or aphenyl group which may be substituted (the substituent is selected from a halogen atom, a group of COOR.sup.10, a nitro group, a lower alkoxy group and a lower alkyl group); R.sup.6 and R.sup.7 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a nitro group or a group of COOR.sup.10 ; R.sup.8 and R.sup.9 each independently represent a hydrogen atom, a lower alkyl group or a phenyl group; W.sup.1 represents an oxygen atom, a sulfur atom or a group of N--R.sup.10 ; R.sup.10 represents a hydrogen atom or a lower alkyl group; R.sup.11 represents a lower alkyl group and n represents an integer of 0, 1 or 2; and R.sup.12 and R.sup.13 each independently represent a hydrogen atom or a lower alkyl group, m represents an integer of 0, 1 or 2; R repesents a hydrogen atom or a lower alkyl group; B and D each independently represent a hydrogen atom, a halogen atom, a nitro group, a lower alkyl group, an aralkyl group, a lower alkoxy group, a halogenated alkyl group, a halogenated alkenyl group, a lower alkoxyalkyl group, an alkylcarbonylgroup, a group of COOR.sup.14, a group of CONR.sup.15 R.sup.16, a group of S(O).sub.n R.sup.17, a cyano group, a group of NR.sup.18 R.sup.19, a group of SO.sub.2 NR.sup.20 R.sup.21 , a hydroxy group, a benzoyl group which may be substituted (thesubstituent is selected from a halogen atom and a lower alkyl group) or a phenyl group which may substituted (the substituent is selected from a halogen atom, a nitro group, a group of COOR.sup.10, a lower alkoxy group and a lower alkyl group); R.sup.14 represents a hydrogen atom, a lower alkyl group which may be substituted (the substituent is selected from a lower alkoxy group which may be substituted by a group of OR.sup.10, a halogen atom, a halogenated lower alkoxy group, a cyanogroup, a phenoxy group, a lower alkoxycarbonyl group, a group of NR.sup.10 R.sup.11, a lower cycloalkyl group, a lower alkylthio group and a lower alkylcarbonyl group), a lower alkenyl group, a halogenated lower alkenyl group, a lower alkynyl group, ahalogenated lower alkynyl group, a halogenated lower cycloalkyl group or a benzyl group; R.sup.15 represents a hydrogen atom, a lower alkyl group or a phenyl group; and R.sup.16 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.17 represents a lower alkyl group, a lower alkoxy group, a phenyl group, a halogenated alkyl group, a lower alkenyloxy group or a lower alkynyloxy group; and n represents an integer of 0, 1 or 2; R.sup.18 and R.sup.19 each independently represent a hydrogen atom, a lower alkyl group, a lower alkylcarbonyl group or a lower alkylsulfonyl group; R.sup.20 and R.sup.21 each independently represent a hydrogen atom, a lower alkyl group, a lower alkenyl group or a lower alkynyl group; T represents a group of ##STR4## E represents a hydrogen atom, a lower alkyl group, a lower alkenyl group, a lower alkynyl group or a lower alkoxy group; G represents a group of; ##STR5## wherein X and Y each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a lower alkoxy group, a lower alkoxyalkyl group, a halogenated alkyl group, a halogenated lower alkoxy group, agroup of NR.sup.24 R.sup.25, a group of OCH(R.sup.10)COOR.sup.10, a group of COOR.sup.10, a cyclopropyl group, a group of CH(OR.sup.26).sub.2, a lower alkylthio group or a halogenated lower alkylthio group, R.sup.24 and R.sup.25 each independently represents a hydrogen atom, a lower alkyl group or a lower alkoxy group; R.sup.26 represents a lower alkyl group; X.sup.1 and Y.sup.1 each independently represent a hydrogen atom, a halogen atom, a lower alkyl group, a halogenated alkyl group or a lower alkoxy group; X.sup.2 represents a lower alkyl group, a lower alkylthio group or a lower alkoxy group, and Y.sup.2 represents a lower alkyl group; Z represents a nitrogen atom or a group of C--R.sup.27, R.sup.27 represents a hydrogen atom, a lower alkyl group, a halogenated lower alkyl group, a halogen atom, a lower alkoxy group or a 5-membered ring structure containing an oxygen atom together with Y or Y.sup.1 ; X.sup.3 represents a lower alkyl group, a lower alkoxy group, a lower alkoxyalkyl group or a halogen atom; Y.sup.3 represents a lower alkyl group, a lower alkoxy group, a halogen atom, a monoalkylamino group or a dialkylamino group; Y.sup.4 represents a cyano group, a group of CO.sub.2 R.sup.10, a nitro group, a group of S(O).sub.n R.sup.11, an alkyl group or a halogenated alkyl group; Z.sup.1 represents a nitrogen atom or a group of CH; X.sup.4 and Y.sup.5 each independently represent a lower alkyl group or a lower alkoxy group; W represents an oxygen atom, a sulfur atom or a group of N--R.sup.28 (wherein R.sup.28 represents a hydrogen atom or a lower alkoxy group); W.sup.2 represents an oxygen atom or a sulfur atom; R.sup.22 represents a lower alkyl group; Az represents a halogen atom, a nitro group, or an imidazolyl group, an imidazolynyl group, a pyrazolyl group, a triazolyl group or a benzimidazolyl group each of which may be mono-, di- or tri-substituted by a lower alkyl group; J represents a lower alkyl group or a group of ##STR6## wherein Q, R, m, B and D have the same meanings as defined above; and R.sup.23 represents a hydrogen atom, a lower alkyl group or a lower alkoxy group, has a strong herbicidal effect to various weeds while retaining high safety to the important crops in either case of the soil treatment or the foliage treatment, whereby this invention has been accomplished. The compound of this invention showsa high herbicidal activity in an application of a very low amount of the active ingredient as compared with the conventional herbicides, and accordingly it is useful also as a herbicide for orchards and uncultivated lands. DESCRIPTION OF THE PREFERRED EMBODIMENTS As a prior technique, for example, Japanese Provisional Patent Publication No. 162587/1983 and No. 1480/1984 disclose imidazolesulfonylurea which has the structure similar to the compound of this invention. However, there has been disclosed nocompound wherein a heterocyclic ring is substituted on an imidazole ring as the compound of this invention. Thus, the compound of this invention can be said to be a novel one. In the present invention, preferred componds represented by the formula (I) are as follows: ##STR7## wherein R.sub.1 represents a hydrogen atom, a methyl group, a halogen atom or a nitro group; R represents a methyl group or an ethyl group; Q isselected from the group of Q5, Q6, Q7, Q9, Q15, Q21, Q26, Q29, Q32, Q50, Q54, Q61, Q68, Q88, Q127, Q138Q142, Q188, Q189, Q201, Q202, Q204, Q205, Q209, Q222, Q225, Q229, Q230, Q246 and Q250 as mentioned on pages 45 to 57 hereinbelow; X and Y are each independently a halogen atom, a methyl group, a methoxy group; and Z is --CH.dbd. or --N.dbd.. The compound of this invention, represented by general formula (I) can be readily prepared by selecting any of reaction schemes 1 to 7 shown below. ##STR8## wherein B, D, E, G, Q, R, W.sup.2 and m have the same meanings as defined above. More specifically, the imidazolesulfonyl(thio)isocyanate derivative (II) is dissolved in a sufficiently dried inert solvent such as dioxane and acetonitrile and thereto is added a pyrimidine, triazine or triazole derivative represented by Formula(III), with stirring. Thus, the reactants generally are reacted with each other rapidly to give the compound (I)' which is part of the compound of this invention. In cases where it is difficult for the reaction to proceed, a trace or small amount ofsuitable base, such as triethylamine, triethylenediamine, pyridine, a sodium alkoxide, sodium hydride and the like, may be added to the reaction system to allow the reaction to proceed readily. ##STR9## wherein B, D, E, G, Q, R, W.sup.2 and m have thesame meanings as defined above. R.sup.29 represents a lower alkyl group or a phenyl group. More specifically, the imidazolesulfonamide derivative (V) is reacted with a chloroformic acid (thio)ester or a carbonic acid (thio)ester in a solvent such as acetone, methyl ethyl ketone and acetonitrile in the presence of a base such aspotassium carbonate to give the compound (IV). Subsequently, the resulting (IV) is heated with the compound (III) in a solvent such as tolune to give the compound (I)' which is a part of the compound of this invention. ##STR10## wherein B, D, E, G, Q,R, W.sup.2 and m have the same meanings as defined above. R.sup.29 represents a lower alkyl group or a phenyl group. More specifically, by reacting the imidazolesulfonamide derivative (V) with an N-heterocylic carbamate (III)' in the presence of an inorganic salts such as hydroxides, hydrides, etc., or an organic bases such as alkylamine, pyridine,1,8-diazabicyclo(5.4.0)-7-undecene in an inert solvent such as methylene chloride, tetrahydrofuran, acetonitrile, etc., the compound (I)' which is a part of the compound of this invention can be obtained. ##STR11## wherein B, D, E, G, Q, R, m, R.sup.22and R.sup.23 have the same meanings as defined above. ##STR12## wherein Az, B, D, E, G, Q, R, W.sup.2, m, R.sup.22 and R.sup.23 have the same meanings as defined above. ##STR13## wherein Az, B, D, E, G, Q, R and m have the same meanings as definedabove. More specifically, the above imidazolesulfonamide derivative in any of Reaction schemes 4 to 6, which is a part of the compound of this invention can be synthesized in accordance with the process disclosed in Japanese Provisional PatentPublications No. 167570/1984, No. 6654/1985, No. 36467/1985, No. 60670/1986, No. 60684/1986 and No. 72783/1986. ##STR14## wherein B, D, E, G, Q, R, W and m have the same meanings as defined above; and Hal represents a halogen atom. More specifically, 1H-imidazolesulfonylurea is reacted with a Hal--(CHR).sub.m --Q in the presence of an appropriate base to give the compound (I)' which is a part of the compound of this invention. Be noted that in case where m is 0, Qdesirably has an electron attractive group such as a nitro group, CF.sub.3, a halogen atom or the like as a substituent therefor in many occasions and the Hal-group is required to have high reactivity. The starting material, the imidazolesulfonyl(thio)isocyanate (II) or the imidazolesulfonyl(thio)carbamate derivative (IV) which is used in Reaction schemes 1 and 2 may be synthesized by optionally selecting the methods as will be describedhereinafter to synthesize the imidazolesulfonamide (V) and further converting the resulting product to the desired product with reference to the methods as described in European Patent Publication No. 87,780 (EP-A0 087 780) and Japanese ProvisionalPatent Publication No. 13266/1980. The imidazolesulfonamide which is an intermediate to be used in the present invention is also a novel compound, which can be obtained by optionally selecting one of the following Reaction schemes 8 to 12 and the methods described in JapaneseProvisional Patent Publications No. 162587/1983, No. 1480/1984, etc. ##STR15## (a) NaNO.sub.2.HCl or NaNO.sub.2.HBr (b) SO.sub.2.Cu salt (c) NH.sub.4 OH or ammonium carbonate (d) Cu salt (e) NaSH (f) NaOH.NH.sub.4 OH/NaOCl (g) Oxidizing agent (h) NaSCH.sub.2 Ph (i) Cl.sub.2 /CH.sub.3 CO.sub.2 H.H.sub.2 O or NaOCl/HCl (j) (1) ClSO.sub.3 H (2) SOCl.sub.2 or PCl.sub.5 (k) (1) BuLi or LiN(i-Pr).sub.2 (2) SO.sub.2 (3) N-chlorosuccinimide (l) Q--(CHR).sub.m --Hal/base In Reaction schemes 8 to 12, B, D, Q, R and m have the same meanings as defined above; and Hal represents a halogen atom. The imidazolesulfonamide (V) may usually be obtained by reacting a corresponding imidazolesulfonyl chloride with an aqueous ammonia or ammonium carbonate. In order to introduce a sulfonyl group into an imidazole ring, there may be adopted suchmethods as follows: (1) The amino group is subjected to diazonium decomposition in the presence of sulfur dioxide to give a imidazolesulfonyl chloride; (2) A sulfur atom is introduced into the imidazole ring by a nucleophilic substitution reaction with a halogen atom or the like and optionally the resulting compound is further oxidized to given an imidazolesulfonyl chloride; (3) A carbanion of an imidazole is formed by using a base and sulfur dioxide is reacted therewith followed by halogenation to give an imidazolesulfonyl chloride; and (4) Chlorosulfonic acid or the like is used to directly give an imdazolesulfonyl chloride in an electrophilic substitution reaction. More specifically, (1) according to Reaction scheme 8, an aminoimidazole is converted into a diazonium salt by using sodium nitrite or the like in hydrochloric acid, hydrobromic acid or the like and then sulfur dioxide is reacted with theresulting diazonium salt in the presence of a catalyst which is usually used for diazonium decomposition such as a copper salt or the like, to afford a corresponding imidazolesulfonyl chloride. With the resulting compound was reacted an aqueous ammoniato give the desired pyrazolesulfonamide (V). (2) According to Reaction scheme 9, a halogenated imidazole is treated with sodium hydrosulfide, sodium salt of benzylmercaptan or the like to introduce a sulfur atom into the imidazole ring, followed by oxidation with chlorine in a solvent suchas acetic acid/water to give an imidazolesulfonyl chloride. As in Reaction scheme 8, a reaction with an aqueous ammonia gives the desired pyrazolesulfonamide (V). The desired imidazolesulfonamide may also be obtained by converting the intermediate ofmercaptopyrazole into a sulfenamide which is then oxidized. The starting material, the halogenated imidazole, may be obtained by diazo-decomposition of an aminopyrazole; by the reaction of a hydroxyimidazole with phosphorus oxychloride or phosphorusoxybromide; or by formation of an anion by using a strong base such as butyl lithium, lithium diisopropylamide or the like, followed by halogenation. (3) According to Reaction scheme 11, an anion may be formed by using a strong base such as butyl lithium, lithium diisopropylamide or the like, and the resulting anion may further be treated with sulfur dioxide and subsequently with anN-halogenosuccinimide to form an imidazolesulfonyl chloride which is then treated with an aqueous ammonia to give the desired imidazolesulfonamide (V). (4) According to Reaction scheme 10, use of chlorosulfonic acid may give directly an imidazolesulfonyl chloride. In addition to the above schemes, according to Reaction scheme 12, the desired imidazolesufonamide (V) may be obtained by allowing an imidazolesulfonamide having no substituent on the 1-position to react with an appropriate halogen derivativeHal--(CHR).sub.m --Q (wherein Q, R, m and Hal have the same meanings as defined above) in the presence of a suitable base. The reaction may be carried out in accordance with Reaction scheme 7. In reactions in Reaction schemes 10 to 12, isomers maypossibly be formed in admixture with the desired compound depending upon occasion. However, such isomers may be separated by recrystallization, column chromatography or the like and used as an intermediate for the compound of this invention. Generalliteratures for the chemistry on the imidazoles used as starting materials in the above-mentioned reactions include the following ones. M. R. Grimmett, Advanced Heterocyclic Chemistry, Vol. 12, p. 104 (1970); R. C. Elderfield, Heterocyclic Compounds,Vol. V, p. 194 (1957), published by John Wiley and Sons, Inc., New York; K. Schofield, M. R. Grimmett and B. R. T. Keene, Heteroaromatic Nitrogen Compounds The Azoles, published by Cambridge University Press, (1976); M. R. Grimmett, ComprehensiveHeterocyclic Chemistry, Vol. 5, p. 345 (1984), published by Pergamon Press. The mercaptoimidazole derivative, for example, may be synthesized, as shown in Reaction scheme 13, according to methods described in R. G. Jones, E. C. Kornfeld, K. C. McLaughlin and R. C. Anderson, J. Am. Chem. Soc., Vol. 71, p. 4000 (1949). ##STR16## wherein Q, R, R.sup.11 and m have the same meanings as defined above; and B and D each independently represent a hydrogen atom or a lower alkyl group. ##STR17## wherein Q, R, R.sup.11, W.sup.2, m and Hal have the same meanings as definedabove; B represents a hydrogen atom, a lower alkyl group or a lower alkylmercapto group; D represents an alkylcarbonyl group, a benzoyl group, a cyano group, an alkylsulfonyl group, a phenylsulfonyl group, a group of COOR.sup.14 or a group of CONR.sup.15R.sup.16 ; wherein R.sup.14, R.sup.15 and R.sup.16 have the same meanings as defined above. ##STR18## wherein Q, R, R.sup.11 and m have the same meanings as defined above; B represents a hydrogen atom or a lower alkyl group; D represents a hydrogenatom, an alkylcarbonyl group, a benzoyl group, a cyano group, an alkylsulfonyl group, a phenylsulfonyl group, a group of COOR.sup.14 or a group of CONR.sup.15 R.sup.16, in which R.sup.14, R.sup.15 and R.sup.16 have the same meanings as defined above. An aminoimidazole may be synthesized, as shown in Reaction scheme 14, according to methods described in K. Gewald and G. Heinhold, Monatsh. Chem., Vol. 107, p. 1413 (1976), specification of East German Pat. No. 118,640 and A. Edenhofer, Helv. Chim. Acta., Vol. 58, p. 2192 (1975) to give 4-aminoimidazole derivatives having various substituents. Also, 5-aminoimidazole may be synthesized, as shown in Reaction scheme 15, according to methods described in D. H. Robinson and G. Shaw, J. Chem.Soc., Perkin Trans. I, p. 1715 (1972). Further, a heterocyclic isothiocyanate which is a raw material to be used in a reaction of Reaction scheme 13 may be synthesized, for example as shown in Reaction scheme 16, according to methods desribed in D. J. LeCount, D. J. Dewsbury and W.Grundy, Synthesis, p. 582 (1977). ##STR19## wherein Q, R and m have the same meanings as defined above. Generally, a person skilled in the art would be able to obtain an intermediate for the compound of the present invention by investigatingexperimental conditions and the like taking into consideration the above descriptions and the prior art technologies as mentioned above. Hereinafter, there will be described Synthesis examples of the present compounds and the intermediateimidazolesulfonamide therefor by way of Examples or Reference examples, which, however, should not be construed to limit the present invention. REFERENCE EXAMPLE 1 Synthesis of 1-methyl-3-pyrazolylisothiocyanate To a mixture of 29.1 g of 3-amino-1-methylpyrazole and 45 ml of triethylamine was added dropwise 18 ml of carbon disulfide and the resulting mixture was stirred at 40.degree. C. for 30 minutes to precipitate solids. To the reaction mixture wasadded ether, followed by pulverization of solids. After filtration, the thus pulverized solids were washed with ether to give 67 g of triethylamine salt of 1-methyl-3-pyrazolyldithiocarbamic acid (melting point: 79.degree. to 82.degree. C.) 31.8 g ofthe thus obtained triethylamine salt of dithiocarbamic acid and 11.7 g of triethylamine were dissolved in 150 ml of methylene chloride. To the resulting solution was added at one time 34.5 g of ferric chloride 6 hydrate dissolved in 100 ml of water,followed by vigorous stirring for 10 minutes. The reaction mixture was filtered to remove insoluble solids. The organic layer was separated and then the aqueous layer was extracted with methylene chloride. After the organic layers were combined,washed with water and dried, the solvent was distilled off under reduced pressure. To the thus obtained residue was added ether to filter the insoluble solids off and the filtrate was concentrated under reduced pressure to give 9.0 g of oil. The thusobtained oil was evaporated under reduced pressure to give 6.5 g of the desired compound. b.p.: 135.degree. to 138.degree. C./23 mmHg. REFERENCE EXAMPLE 2 Synthesis of 1-(1-methylpyrazol-3-yl)imidazole-2-thiol To 6.6 g of 2,2-diethoxyethylamine dissolved in 100 ml of ethanol was added 6.3 g of 1-methyl-3-pyrzolylisothiocyanate, followed by stirring at room temperature over night. Crystals precipitated were filtered out and washed with a small amountof ethanol to give 10.3 g of N-2,2-diethoxyethyl-N'-(1-methylpyrazol-3-yl)thiourea (m.p.: 152.degree. to 155.degree. C.). 10.0 g of the crystals thus obtained were suspended in 70 ml of water. To the resulting suspension was added 15 ml of conc.hydrochloric acid, followed by stirring under reflux with heating for 30 minutes. The reaction mixture was cooled and adjusted to pH to 4 to 6 with use of 50% aqueous sodium hydroxide solution to precipitate crystals. The crystals precipitated werefiltered out, washed with water and dried to give 6.0 g of the desired compound. m.p.: 126.degree. to 128.degree. C. REFERENCE EXAMPLE 3 Synthesis of 1-(4-chloro-1-methylpyrazol-3-yl)imidazole- 2-sulfonamide To a mixture of 5.8 g of 1-(1-methylpyrazol-3-yl)imidazole-2-thiol, 30 ml of water, 60 ml of chloroform and 27 g of conc. hydrochloric acid was added dropwise 192 g of aqueous sodium hypochlorite solution (content of 6%) under vigorous stirringat -10.degree. to 0.degree. C. over about 4 hours. After completion of the dropwise addition, the resulting mixture was stirred at the same temperature for 1 hour. Then, the organic layer was separated and the aqueous layer was extracted withchloroform. The organic layers were combined and washed with water. Then, to the organic layer was added dropwise 20 ml of 28% aqueous ammonia under ice-cooling, followed by stirring at room temperature for 1.5 hours. Crystals precipitated byconcentrating the resulting mixture under reduced pressure, were filtered out, washed with water and subsequently with ether to give 2.9 g of the desired compound. m.p.: 208.degree. to 210.degree. C. REFERENCE EXAMPLE 4 Synthesis of 1-methyl-5-pyrazolylisothiocyanate Using 5-amino-1-methylpyrazole as a starting material, triethylamine salt of 1-methyl-5-pyrazolyldithiocarbamic acid (m.p.: 89.degree. to 94.degree. C.) was synthesized, following the procedures described in Reference Example 1. Ferricchloride was allowed to act upon the resulting product to yield the desired compound. Oily substance. REFERENCE EXAMPLE 5 Synthesis of 1-(1-methylpyrazol-5-yl)imidazole-2-thiol Using 1-methyl-5-pyrazolylisothiocyanate as a starting material, the desired compound was obtained via N-2,2-diethoxyethyl-N'-(1-methylpyrazol-5-yl)thiourea (m.p.: 148.degree. to 149.degree. C.) as an intermediate, following the proceduresdescribed in Reference Example 2. m.p.: 247.degree. to 251.degree. C. REFERENCE EXAMPLE 6 Synthesis of 1-(1-methylpyrazol-5-yl)imidazole-2-sulfonamide To a mixture of 5.0 g of 1-(1-methylpyrazol-5-yl)imidazole-2-thiol, 30 ml of water, 60 ml of chloroform and 23 g of conc. hydrochloric acid, was added dropwise 100 g of aqueous sodium hypochlorite (content of 6%) under vigorous stirring at-10.degree. to 0.degree. C. over 2.5 hours. After completion of the dropwise addition, the resulting mixture was stirred at the same temperature for 0.5 hour. Then the organic layer was separated and the aqueous layer was extracted with chloroform. After the organic layers were combined and washed with water, to the organic layer was added dropwise 20 ml of 28% aqueous ammonia under ice-cooling, followed by stirring at room temperature for 1.5 hours. Crystals precipitated by concentrating theresulting mixture under reduced pressure, were filtered out, washed with water and subsequently with ether to give 3.4 g of the desired compound. m.p.: 230.degree. to 233.degree. C. REFERENCE EXAMPLE 7 Synthesis of 5-amino-4-ethoxycarbonyl-1-(1-methylpyrazol-3-yl)imidazole In 200 ml of acetonitrile, 6.7 g of ethyl-aminocyanoacetate, 8.5 g of ethyl orthoformate and 5.6 g of 3-amino-1-methylpyrazole were refluxed under heating for 4.5 hours. After completion of the reaction, the solvent was distilled off underreduced pressure. Crystals precipitated was filtered out, followed by washing with ether to give 7.5 g of the desired compound. m.p.: 168.degree. to 170.degree. C. REFERENCE EXAMPLE 8 Synthesis of 5-chloro-4-ethoxycarbonyl-1-(1-methylpyrazol-3-yl)imidazole 7.4 g of 5-amino-4-ethoxycarbonyl-1-(1-methylpyrazol-3-yl)imidazole was dissolved in 40 ml of conc. hydrochloric acid and the resulting solution was cooled to -5.degree. C. Subsequently, 2.6 g of sodium nitrite was dissolved in 10 ml of waterand the resulting solution was added dropwise to the previously prepared solution while maintaining the temperature at -5.degree. C. or lower. After completion of the dropwise addition, the resulting mixture was stirred at the same temperature for 0.5hour. The thus obtained solution was added dropwise at around 5.degree. C. to 120 ml of a solution of chloroform containing 0.5 g of cuprous chloride and 17 g of sulfur dioxide. After the resulting mixture was stirred at room temperature for 1 hour,was added thereto 200 ml of water and the organic layer was separated. The aqueous layer was extracted with chloroform and the organic layers were combined, washed with water and dried. The solvent was then removed by distillation to give 8.0 g of5-chloro-6-ethoxycarbonyl-1-(1-methylpyrazol- 3-yl)imidazole as an oil. REFERENCE EXAMPLE 9 Synthesis of 1-(4-chloro-1-methylpyrazol-3-yl)-4-ethoxycarbonylimidazole-5-sulfonamide 7.5 g of 5-chloro-4-ethoxycarbonyl-1-(1-methylpyrazol-3-yl)imidazole was dissolved in 30 ml of dimethylformamide. To the resulting solution was added 5.9 g of sodium hydrosulfide (content of 70%), followed by stirring of the resulting mixture at70.degree. to 80.degree. C. for 1.5 hours. After completion of the reaction, 100 ml of ice-cold water was added to the reaction mixture and the resulting mixture was made weakly acidic with use of conc. hydrochloric acid. Subsequently, 100 ml ofchloroform was added to the mixture and chlorine was introduced into the resulting mixture little by little at -10.degree. to 0.degree. C. over 2 hours. After completion of the reaction, the organic layer was separated and the aqueous layer wasextracted with chloroform. After the organic layers were combined and washed with water, 20 ml of 28% aqueous ammonia was added dropwise under ice-cooling, followed by stirring of the resulting mixture at room temperature for 1.5 hours. Crystalsprecipitated by concentrating the reaction mixture under reduced pressure were filtered out and washed with water and subsequently with ether to give 7.6 g of the desired compound. m.p.: 167.degree. to 168.degree. C. REFERENCE EXAMPLE 10 Synthesis of 5-amino-4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole Following the procedure described in Reference Example 7, the desired compound was synthesized using ethyl .alpha.-aminocyanoacetate, ethyl orthoformate and 2-aminothiazole as raw materials. m.p.: 120.degree. to 123.degree. C. REFERENCE EXAMPLE 11 Synthesis of 5-chloro-4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole Following the procedure described in Reference Example 8, the desired compound was synthesized using 5-amino-4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole as a raw material. m.p.: 128.degree. to 131.degree. C. REFERENCE EXAMPLE 12 Synthesis of 4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole-5-thiol 8.0 g of 5-chloro-4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole was dissolved in 30 ml of dimethylformamide. To the resulting solution was added 6.2 g of sodium hydrosulfide (content of 70%), followed by stirring of the resulting mixture at60.degree. C. for 1 hour. After completion of the reaction, the reaction mixture was poured into ice water and the resulting solution was made weakly acidic with conc. hydrochloric acid. Crystals precipitated were filtered out, washed and dried togive 7.5 g of the desired compound. m.p.: 155.degree. to 158.degree. C. REFERENCE EXAMPLE 13 Synthesis of 4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole-5-sulfonamide The desired compound was synthesized following the procedures described in Reference Example 6 by using 4-ethoxycarbonyl-1-(thiazol-2-yl)imidazole-5-thiol as a raw material. m.p.: 84.degree. to 85.degree. C. REFERENCE EXAMPLE 14 Synthesis of 5-amino-4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole The desired compound was synthesized following the procedures described in Reference Example 7 by using ethyl .alpha.-aminocyanoacetate, ethyl orthoformate and 2-amino-4-methylthiazole as raw materials. m.p.: 152.degree. to 155.degree. C. REFERENCE EXAMPLE 15 Synthesis of 5-chloro-4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole The desired compound was synthesized following the procedures described in Reference Example 8 by using 5-amino-4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole as a raw material. m.p.: 98.degree. to 101.degree. C. REFERENCE EXAMPLE 16 Synthesis of 4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole-5-thiol The desired compound was synthesized following the procedures described in Reference Example 12 by using 5-chloro-4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole as a raw material. m.p.: 193.degree. to 195.degree. C. REFERENCE EXAMPLE 17 Synthesis of 4-ethoxycarbonyl-1-(5-chloro-4-methylthiazol-2-yl)imidazole-5-sulfonamide A mixture consisting of 4.2 g of 4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole-5-thiol, 3.2 g of anhydrous potassium carbonate, 2.2 g of benzyl chloride, 20 ml of dimethylformamide and 100 ml of acetonitrile was stirred at room temperaturefor 2 hours. After the reaction, solid materials were separated by filtration, and the filtrate was condensed under reduced pressure to obtain crude 5-benzylthio-4-ethoxycarbonyl-1-(4-methylthiazol-2-yl)imidazole as oily product. The resulting oilyproduct was dissolved in 100 ml of chloroform and after addition of 13 g of conc. hydrochloric acid and 30 ml of water, 28 g of a 10% sodium hypochlorite solution was added dropwise to the mixture at -10.degree. C. to -5.degree. C. over 15 minutes. After the reaction mixture was stirred at 0.degree. C. or lower for 20 minutes, an organic layer was separated and an aqueous layer was extracted with chloroform. After the organic layers were combined and washed with water, 60 ml of tetrahydrofuranwas added to the organic layer and then 20 ml of a 28% aqueous ammonia was added dropwise under icc-cooling, and the mixture was stirred at room temperature for 1.5 hours. After the reaction mixture was concentrated under reduced pressure, ethyl acetateand water were added thereto, an organic layer was separated and an aqueous layer was extracted with ethyl acetate. The organic layers were combined and dried, and then concentrated under reduced pressure to obtain oily product. The resulting oilyproduct was identified as 5-benzylsulfinyl-4-ethoxycarbonyl-1-(5-chloro-4-methylthiazol-2-yl)imidazo le by NMR and MS analyses. The resulting oily product was again treated with sodium hypochlorite in accordance with the above-mentioned method, and reacted with an aqueous ammonia to obtain 0.86 g of the title compound. m.p.: 136.degree. to 139.degree. C. REFERENCE EXAMPLE 18 Synthesis of 5-amino-4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole The desired compound was synthesized following the procedures described in Reference Example 7 by using ethyl .alpha.-aminocyanoacetate, ethyl orthoformate and 2-amino-1,3,4-thiadiazole as raw materials. m.p.: 181.degree. to 183.degree. C. REFERENCE EXAMPLE 19 Synthesis of 5-chloro-4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole The desired compound was synthesized following the procedures described in Reference Example 8 by using 5-amino-4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole as a raw material. m.p.: 184.degree. to 185.degree. C. REFERENCE EXAMPLE 20 Synthesis of 4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole-5-thiol The desired compound was synthesized following the procedures described in Reference Example 12 by using 5-chloro-4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole as a raw material. m.p.: 182.degree. to 185.degree. C. REFERENCE EXAMPLE 21 Synthesis of 4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole-5-sulfonamide The desired compound was synthesized following the precedures described in Reference Example 17 by using 4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole-5-thiol as a raw material and via 5-benzylthio-4-ethoxycarbonyl-b1-(1,3,4-thiadiazol-2-yl)imidazole (m.p.: 113.degree. to 115.degree. C.) as an indermediate. m.p.: 168.degree. to 171.degree. C. REFERENCE EXAMPLE 22 Synthesis of 1-(thiazol-2-yl)imidazole-2-thiol To 200 ml of acetonitrile, 14.6 g of N-(thiazol-2-yl)methyldithiocarbamate and 12 g of 2,2-diethoxyethylamine were added and the mixture was refluxed under heating for 12 hours. After removing acetonitrile, diisopropyl ether was added to theresidue and precipitated crystals were collected by filtration to obtain 9.5 g of N-2,2-diethoxyethyl-N'-(thiazol-2-yl)thiourea (m.p.: 118.degree. to 119.degree. C.). In 55 ml of water was suspended 8.5 g of the resulting crystals, and 25 ml of conc.hydrochloric acid was added thereto and then the mixture was refluxed under heating for 5 hours. The reaction mixture was cooled and then the precipitated crystals were collected by filtration. The resulting crystals were dissolved in 30 ml of a 20%aqueous sodium hydroxide solution and a pH thereof was adjusted to 7 to 6 to precipitate crystals. The precipitated crystals were collected by filtration, washed with water and then dried to obtain 5.0 g of the title compound. m.p.: 211.degree. to213.degree. C. REFERENCE EXAMPLE 23 Synthesis of 1-(thiazol-2-yl)imidazole-2-sulfonamide The desired compound was synthesized following the procedures described in Reference Example 6 by using 1-(thiazol-2-yl)imidazole-2-thiol as a raw material. m.p.: 157.degree. to 162.degree. C. REFERENCE EXAMPLE 24 Synthesis of 1-(2-pyridyl)imidazole-2-sulfonamide (1) Synthesis of 1-(2-pyridyl)imidazole-2-thiol To a solution of 11.1 g of 2-pyridylisothiocyanate dissolved in 100 ml of ethanol, was added 10.0 g of aminoacetaldehyde diethylacetal, followed by stirring of the resulting mixture under reflux with heating for 40 minutes. After completion ofthe reaction, the solvent was distilled off under reduced pressure. Crystals precipitated were collected by filtration to give 13.8 g of N-2,2-diethoxyethyl-N'-(2-pyridyl)thiourea (m.p.: 132.degree. to 133.degree. C.). To the thus obtained crystalswas added 120 ml of 10% diluted hydrochloric acid, followed by stirring of the resulting mixture under reflux with heating for 30 minutes. The reaction mixture was cooled and adjusted to pH of 5 to 6 with use of 50% aqueous sodium hydroxide toprecipitate crystals. The crystals precipitated were filtered out, washed with water and dried to give 8.3 g of the desired compound. m.p.: 162.degree. to 163.degree. C. (2) Synthesis of 1-(2-pyridyl)imidazole-2-sulfonamide A mixture consisting of 5.1 g of 1-(2-pyridyl)imidazole-2-thiol, 5.2 g of anhydrous potassium carbonate, 3.7 g of benzyl chloride and 50 ml of acetonitrile was stirred at room temperature for 4 hours. After completion of the reaction, solidswere filtered off and the filtrate was concentrated under reduced pressure. Crystals precipitated were collected by filtration to give 7.1 g of 2-benzylthio-1-(2-pyridyl)imidazole (m.p.: 76.degree. to 77.degree. C.). To a mixture consisting of 7.1 gof the thus obtained crystals, 50 ml of methylene chloride, 50 ml of water and 22 g of conc. hydrochloric acid was added dropwise 80 g of 6% sodium hypochlorite solution under vigorous stirring at -10.degree. to 0.degree. C. over 1 hour. Aftercompletion of the dropwise addition, the resulting mixture was stirred at the same temperature for 30 minutes. Then, the organic layer was separated and the aqueous layer was extracted with methylene chloride. After the organic layers were combined andwashed with water, to the organic layer was added dropwise 10 ml of a 28% aqueous ammonia under ice-cooling while vigorous stirring. After completion of the dropwise addition, the resulting mixture was stirred at room temperature for 1.5 hours. Thereaction mixture was concentrated to dryness and the thus obtained concentrated residue was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure to give 3.0 g of a crude product of the desired compound. Crystalsprecipitated from the resulting crude product were collected by filtration to give 0.8 g of the desired compound. m.p.: 187.degree. to 188.degree. C. REFERENCE EXAMPLE 25 Synthesis of 4-ethoxycarbonyl-1-(2-pyridyl)imidazole-5-sulfonamide (1) Synthesis of 5-amino-4-ethoxycarbonyl-1-(2-pyridyl)imidazole In 230 ml of acetonitrile, 8.5 g of ethyl .alpha.-aminocyanoacetate, 10.8 g of ethyl orthoformate and 6.2 g of 2-aminopyridine were heated under reflux for 1.5 hours. After completion of the reaction, the solvent was distilled off under reducedpressure and crystals precipitated were filtered off and washed with benzene to give 11.0 g of the desired compound. m.p.: 129.degree. to 131.degree. C. (2) Synthesis of 4-ethoxycarbonyl-1-(2-pyridyl)imidazole-5-thiol 11.0 g of 5-amino-4-ethoxycarbonyl-1-(2-pyridyl)imidazole was dissolved in 60 ml of conc. hydrochloric acid and the resulting solution was cooled to -5.degree. C. Subsequently, 3.9 g of sodium nitrite was dissolved in 10 ml of water and theresulting solution was added dropwise to the previously prepared solution while maintaining the temperature at -5.degree. C. or lower. After completion of the dropwise addition, the resulting mixture was stirred at the same temperature for 0.5 hour. The thus obtained solution was added dropwise at around 5.degree. C. to 150 ml of a solution of chloroform containing 1.0 g of cuprous chloride and 12 g of sulfur dioxide. After the resulting mixture was stirred at room temperature for 1 hour, wasadded thereto 300 ml of water and the organic layer was separated. The aqueous layer was extracted with chloroform and the organic layers were combined, washed with water and dried. The solvent was then removed by distillation to give 11.6 g of5-chloro-4-ethoxycarbonyl-1-(2-pyridyl)imidazole as an oil. The thus obtained 11.6 g of 5-chloroimidazole derivative was dissolved in 30 ml of dimethylformamide. To the resulting solution was added 9.2 g of sodium hydrosulfide (content of 70%), followed by stirring of the resulting mixture at roomtemperature for 1 hour. The reaction mixture was poured into ice water and insolubles were filtered out. Then the filtrate was made weakly acidic with use of conc. hydrochloric acid. Crystals precipitated were collected by filtration, washed withwater and dried to give 10.6 g of the desired compound. m.p.: 84.degree. to 87.degree. C. (3) Synthesis of 4-ethoxycarbonyl-1-(2-pyridyl)imidazole-5-sulfonamide To a mixture consisting of 10.6 g of 4-ethoxycarbonyl-1-(2-pyridyl)imidazole-5-thiol, 50 ml of water, 100 ml of chloroform and 35.5 g of conc. hydrochloric acid, was added dropwise 128 g of sodium hypochlorite solution (content of 6%) undervigorous stirring at -10.degree. to 0.degree. C. over 1 hour. After completion of the dropwise addition, the resulting mixture was stirred at the same temperature for 0.5 hour. Then, the organic layer was separated and the aqueous layer was extractedwith chloroform. After the organic layers were combined and washed with water, to the organic layer was added dropwise 10 ml of 28% aqueous ammonia under ice-cooling, followed by stirring of the resulting mixture at room temperature for 1.5 hours. Thereaction mixture was concentrated to dryness under reduced pressure and the residue was extracted with ethyl acetate. After the solvent was distilled off, crystals precipitated were collected by filtration to give 4.1 g of the desired compound. m.p.: 138.degree. to 139.degree. C. Specific examples of synthesizing the present compounds using the intermediate obtained in the above Reference Examples will be given below. EXAMPLE 1 Synthesis of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-(4-chloro-1-methylpyrazol -3-yl)imidazole-2-sulfonamide In 50 ml of acetonitrile, 2.8 g of 1-(4-chloro-1-methylpyrazol-3-yl)imidazole-2-sulfonamide, 1,4 g of ethyl chloroformate and 2.2 g of anhydrous potassium carbonate were heated under reflux for 2 hours. After completion of the reaction, thesolvent was removed by distillation under reduced pressure and ice water was added to the residue and then extracted with chloroform. The aqueous layer was separated and was made acidic with diluted hydrochloric acid. Crystals thus precipitated werefiltered, washed with water and dried to give 2.1 g of N-[1-(4-chloro-1-methylpyrazol-3-yl)imidazole-2-sulfonyl]ethyl carbamate. m.p.: 150.degree. to 151.degree. C. 0.7 g of ethyl carbamate thus obtained and 0.32 g of 2-amino-4,6-dimethoxypyrimidine were refluxed under heating in 30 ml of toluene for 2 hours while removing toluene by distillation little by little. After completion of the reaction, theresidue was left for cooling and crystals precipitated were filtered out and washed with benzene to give 0.6 g of the desired compound. m.p.: 164.degree. to 165.degree. C. EXAMPLE 2 Synthesis of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-1-(2-pyridyl)imidazole-2-su lfonamide In 15 ml of acetonitrile, 0.8 g of 1-(2-pyridyl)imidazole-2-sulfonamide, 0.5 g of methyl chloroformate and 0.75 g of anhydrous potassium carbonate were refluxed under heating for 1 hour. After the reaction, the solvent was removed bydistillation under reduced pressure and ice water was added to the residue, followed by extraction with methylene chloride. The aqueous layer was made weakly acidic with use of diluted hydrochloric acid and concentrated under reduced pressure toprecipitate crystals. Crystals thus precipitated were filtered, washed with water and dried to give 0.46 g of N-[1-(2-pyridyl)imidazole-2-sulfonyl]methyl carbamate. m.p.: 154.degree. to 156.degree. C. 0.46 g of methyl carbamate thus obtained and 0.25 g of 2-amino-4,6-dimethoxypyrimidine were refluxed under heating in 30 ml of toluene for 1.5 hours while removing toluene little by little by distillation. After the reaction, the filtration wascarried out during hot. Crystals precipitated from the filtrate were filtered out to give 0.3 g of the desired compound. m.p.: 146.degree. to 149.degree. C. EXAMPLE 3 Synthesis of N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]-4-ethoxycarbonyl-1-(1,3,4-t hiadiazol-2-yl)imidazole-5-sulfonamide 0.23 g of 1,8-diazobicyclo(5,4,0)-7-undecene was added dropwise to a mixture of 0.45 g of 4-ethoxycarbonyl-1-(1,3,4-thiadiazol-2-yl)imidazole-5-sulfonamide, 0.41 g of N-(4,6-dimethoxypyrimidine-2-yl)phenylcarbamate and 5 ml of acetonitrile. After stirring the reaction mixture at room temperature for 20 minutes, 20 ml of ice water was added thereto and the mixture was filtered. The filtrate was made acidic with use of conc. hydrochloric acid, and resulting precipitated crystals werecollected by filtration, washed with water and ethyl ether, and dried to obtain 0.45 g of the title compound. m.p.: 169.degree. to 171.degree. C. Chemical structures and physical properties of compounds synthesized according to Examples in addition to the compound synthesized in Examples will be given below. ##STR20## Examples of compounds to be included in the compound of this invention are shown below in Table 1 to Table 15 in addition to the compounds synthesized in the above Example, which, however, should not be construed to limit this invention. Be noted that the symbols in Tables have the meanings as shown below. Me: methyl group, Et: ethyl group, Pr-n: n-propyl group, Pr-i: isopropyl group, Ph: phenyl group Gn represents the following groups. Ga=G1 to G35, Gb=G1 to G6, Gc=G1 to G3 ##STR21## Qn have the following meanings. ##STR22## J1 to J14 each represent the following groups. ##STR23## TABLE 1 ______________________________________ A B D Gn ______________________________________ Q1 H H Gb CH.sub.2 - Q1 H H Gc CHMe- Q1 H H G3 Q2 H H Gb Q3 H H Gb Q4 H H Gb Q5 H H Ga CH.sub.2 - Q5 H H Gc CHMe - Q5 H H G3 Q6 H H G3 Q7H H G3 Q8 H H G3 Q9 H H Gc CH.sub.2 - Q9 H H Gc Q10 H H Gc Q11 H H G3 Q12 H H G3 Q13 H H G3 Q14 H H G1 Q15 H H G3 Q16 H H Gc Q17 H H Gc Q18 H H G3 Q19 H H Gc Q20 H H Gc Q21 H H Gc Q22 H H G3 Q23 H H Gc CH.sub.2 - Q23 H H G3 Q24 H H Gc Q25 H H Gb Q26 H H Gb CH.sub.2 - Q26 H H G3 CHMe - Q26 H H G3 Q27 H H G3 Q28 H H G3 Q29 H H Gc CH.sub.2 - Q29 H H G3 Q30 H H G3 Q31 H H Gc Q32 H H Gc CH.sub.2 - Q32 H H G3 Q33 H H G3 Q34 H H G3 Q35 H H G3 Q36 H H G3 Q37 H H Gc Q38 H H Gc Q39 H H G3 Q40 H H Gc Q41 H H Gc Q42 H H Gc Q43 H H G3 Q44 H H Gc Q45 H H Gc Q46 H H Gc Q47 H H Gc Q48 H H Gc Q49 H H G3 Q50 H H Gc CH.sub.2 - Q50 H H G3 Q51 H H Gc Q52 H H G3 Q53 H H G3 Q54 H H Gc Q55 H H Gc Q56 H H Gc Q57 H H G3 Q58H H Gc Q59 H H Gc CH.sub.2 - Q59 H H G3 Q60 H H Gc Q61 H H Ga CH.sub.2 - Q61 H H Gb CHMe - Q61 H H Gc Q62 H H Gc Q63 H H Gc Q64 H H Gb CH.sub.2 - Q64 H H G3 CHMe - Q64 H H G3 Q65 H H G3 Q66 H H G3 Q67 H H G3 Q68 H H G3 Q69 H H Gc Q70 H HGc Q71 H H Gc Q72 H H Gc CH.sub.2 - Q72 H H G3 CHMe - Q72 H H G3 Q73 H H Gc CH.sub.2 - Q73 H H G3 Q74 H H Gc Q75 H H G3 Q76 H H G3 Q77 H H Gc CH.sub.2 - Q77 H H G3 Q78 H H Gc Q79 H H Gc Q80 H H Gc Q81 H H G3 Q82 H H G3 Q83 H H G1 Q84 HH G2 Q85 H H G3 Q86 H H Gc Q87 H H G2 Q88 H H Gc Q89 H H Gc Q90 H H Gc Q91 H H Gc Q92 H H G3 Q93 H H Gc Q94 H H G3 Q95 H H Gc Q96 H H G3 Q97 H H Gc Q98 H H Gc Q99 H H Gc Q100 H H Gc Q101 H H Gc CH.sub.2 - Q101 H H G3 Q102 H H G3 Q103H H G3 Q104 H H G3 Q105 H H Gc Q106 H H G3 Q107 H H Gc Q108 H H G1 Q109 H H G3 Q110 H H G3 Q111 H H G3 Q112 H H Gc Q113 H H Gc Q114 H H Gc Q115 H H G2 Q116 H H Gc Q117 H H Gc Q118 H H G3 Q119 H H Gc Q120 H H Gc Q121 H H G2 Q122 H H Gc Q123 H H Gc Q124 H H Gc Q125 H H Gc Q126 H H Gc Q127 H H Gc Q128 H H Gc Q129 H H Gc Q130 H H G2 Q131 H H Gc Q132 H H Gc Q133 H H G3 Q134 H H G3 Q135 H H Gc Q136 H H G3 Q137 H H G1 Q138 H H Gc CH.sub.2 - Q138 H H G3 Q139 H H G3 Q140 H HG1 Q141 H H G3 Q142 H H Gc Q143 H H Gc CH.sub.2 - Q143 H H G3 Q144 H H G3 Q145 H H Gc Q146 H H Gc Q147 H H G3 Q148 H H G1 Q149 H H G3 Q150 H H G3 Q151 H H G2 Q152 H H G1 Q153 H H Gc Q154 H H Gc Q155 H H G3 Q156 H H G3 Q157 H H Gc Q158H H Gc CH.sub.2 - Q158 H H G3 CHMe - Q158 H H G3 Q159 H H G3 Q160 H H Gc Q161 H H Gc Q162 H H Gc Q163 H H G3 Q164 H H Gc Q165 H H Gc Q166 H H Gc Q167 H H G3 Q168 H H G3 Q169 H H Gc CH.sub.2 - Q169 H H G3 CHMe - Q169 H H G3 Q170 H H Gc Q171 H H Gc Q172 H H Gc Q173 H H Gc Q174 H H Gc Q175 H H Gc Q176 H H Gc Q177 H H Gc CH.sub.2 - Q177 H H G3 CHMe - Q177 H H G3 Q178 H H G3 Q179 H H G3 Q180 H H Gc CH.sub.2 - Q180 H H G3 Q181 H H G1 Q182 H H G3 Q183 H H G3 Q184 H H Gc CH.sub.2 - Q184 H H G3 CHMe - Q184 H H G3 Q185 H H G3 Q186 H H G3 Q187 H H G3 Q188 H H Gb Q189 H H Gb Q1 H Me G3 Q2 H Me G3 Q4 H Me G3 Q5 H Me G3 Q7 H Me G3 Q9 H Me G3 Q10 H Me G3 Q19 H Me G3 Q23 H Me G3 Q26 H Me G3 Q32 H Me G3 Q41 HMe G3 Q45 H Me G3 Q50 H Me G3 Q61 H Me G3 Q69 H Me G3 Q79 H Me G3 Q83 H Me G3 Q96 H Me G3 Q124 H Me G3 Q131 H Me G3 Q132 H Me G3 Q135 H Me G3 Q138 H Me G3 Q142 H Me G3 Q157 H Me G3 Q158 H Me G3 Q159 H Me G3 Q177 H Me G3 Q180 H Me G3 Q184 H Me G3 Q188 H Me Gb Q189 H Me Gb Q1 Me H G3 Q2 Me H G3 Q4 Me H G3 Q5 Me H G3 Q7 Me H G3 Q9 Me H G3 Q10 Me H G3 Q19 Me H G3 Q23 Me H G3 Q26 Me H G3 Q32 Me H G3 Q41 Me H G3 Q45 Me H G3 Q50 Me H G3 Q61 Me H G3 Q69 Me H G3 Q79 Me H G3 Q83 Me H G3 Q96 Me H G3 Q124 Me H G3 Q131 Me H G3 Q132 Me H G3 Q135 MeH G3 Q138 Me H G3 Q142 Me H G3 Q157 Me H G3 Q158 Me H G3 Q159 Me H G3 Q177 Me H G3 Q180 Me H G3 Q184 Me H G3 Q188 Me H Gb Q189 Me H Gb Q4 Me Me G3 Q5 Me Me G3 Q7 Me Me G3 Q9 Me Me G3 Q23 Me Me G3 Q26 Me Me G3 Q32 Me Me G3 Q61 Me Me G3 Q96 Me Me G3 Q142 Me Me G3 Q158 Me Me G3 Q188 Me Me Gb Q189 Me Me Gb Q201 H H Ga CH.sub.2 - Q201 H H Ga CHMe - Q201 H H Gc Q202 H H Gb Q203 H H Gb Q204 H H Gb Q205 H H Gb CH.sub.2 - Q205 H H Gc Q206 H H G3 Q207 H H Gc Q208 H H G3 Q209 HH Gc CH.sub.2 - Q209 H H Gc Q210 H H Gc Q211 H H G3 Q212 H H Gc Q213 H H Gc Q214 H H G1 Q215 H H Gc Q216 H H Gc Q217 H H Gc Q218 H H G3 Q219 H H Gc Q220 H H Gc Q221 H H G2 Q222 H H Gb CH.sub.2 - Q222 H H Gc Q223 H H G3 Q224 H H Gc Q225 H H Gb CH.sub.2 - Q225 H H Gc Q226 H H G3 Q227 H H Gc Q228 H H Gc Q229 H H Gb CH.sub.2 - Q229 H H Gc Q230 H H Gc Q231 H H Gc CH.sub.2 - Q231 H H Gc Q232 H H Gc Q233 H H G3 Q234 H H Gc Q235 H H Gc Q236 H H G1 Q237 H H Gc Q238 H HGc Q239 H H G3 Q240 H H Gc Q241 H H Gc Q242 H H Gc Q243 H H G3 Q244 H H Gc Q245 H H Gc Q246 H H Gb CH.sub.2 - Q246 H H Gc Q247 H H Gc Q248 H H G2 Q249 H H Gc Q250 H H Gc CH.sub.2 - Q250 H H Gc Q251 H H Gc Q252 H H G3 Q253 H H Gc Q254H H Gc Q255 H H Gc Q256 H H G2 Q257 H H Gc Q258 H H Gc Q259 H H Gc CH.sub.2 - Q259 H H G3 Q260 H H Gc CH.sub.2 - Q60 H H Gc Q261 H H G1 Q262 H H Gc Q263 H H Gc Q264 H H G1 Q201 H Me Gc Q202 H Me G3 Q205 H Me Gc Q209 H Me G1 Q222 H Me Gc Q225 H Me G3 Q229 H Me Gc Q231 H Me Gc Q246 H Me G3 Q260 H Me Gc Q201 Me H Gc Q202 Me H G3 Q205 Me H Gc Q209 Me H Gc Q222 Me H Gc Q225 Me H G2 Q229 Me H Gc Q231 Me H Gc Q246 Me H G1 Q260 Me H Gc Q201 Me Me Gc Q202 Me Me G3 Q205 Me Me Gc Q209 Me Me G3 Q222 Me Me Gc Q225 Me Me Gc Q229 Me Me Gc Q231 Me Me G1 Q246 Me Me Gc Q260 Me Me G3 Q201 C1 H Gc Q205 C1 H Gc Q222 C1 H G3 Q229 C1 H Gc Q201 H C1 Gc Q205 H C1 G1 Q201 C1 Me Gc Q205 C1 Me Gc Q201 C1 C1 Gc Q205 C1 C1 Gc Q222C1 C1 G3 Q229 C1 C1 Gc Q201 Br H Gc Q205 Br H Gc Q222 Br H G2 Q229 Br H Gc Q201 H Br Gc Q205 H Br G3 Q201 Br Me Gc Q205 Br Me G3 Q201 Br Br Gc Q205 Br Br G3 Q6 H Me Gb Q15 H Me Gc Q21 H Me G3 Q29 H Me Gb Q54 H Me Gb Q68 H Me Gb Q88 H MeG3 Q127 H Me G3 Q204 H Me G3 Q230 H Me G3 Q250 H Me G3 Q5 H C1 G3 Q6 H C1 G3 Q7 H C1 G3 Q9 H C1 G3 Q15 H C1 G3 Q21 H C1 G3 Q26 H C1 G3 Q29 H C1 G3 Q32 H C1 G3 Q50 H C1 G3 Q54 H C1 G3 Q61 H C1 G3 Q68 H C1 G3 Q88 H C1 G3 Q127 H C1 G3 Q138 H C1 G3 Q142 H C1 G3 Q188 H C1 G3 Q189 H C1 G3 Q202 H C1 G3 Q204 H C1 G3 Q209 H C1 G3 Q222 H C1 G3 Q225 H C1 G3 Q229 H C1 G3 Q230 H C1 G3 Q246 H C1 G3 Q250 H C1 G3 Q5 H NO.sub.2 G3 Q6 H NHCOMe G3 Q7 H NO.sub.2 G3 Q9 H NO.sub.2 G3 Q15 H NMe.sub.2 G3 Q21 H NMe.sub.2 G3 Q26 H NHCOMe G3 Q29 H NO.sub.2 G3 Q32 H NMe.sub.2 G3 Q50 H NO.sub.2 G3 Q54 H NMe.sub.2 G3 Q61 H NO.sub.2 G3 Q68 H NO.sub.2 G3 Q88 H NO.sub.2 G3 Q127 H NMe.sub.2 G3 Q138 H NHCOMe G3 Q142 H NO.sub.2 G3 Q188 H NO.sub.2 G3 Q189 H NO.sub.2 G3 Q201 H NMe.sub.2 G3 Q202 H NHCOMe G3 Q204 H NO.sub.2 G3 Q205 H NHCOMe G3 Q209 H NMe.sub.2 G3 Q222 H NO.sub.2 G3 Q225 HNMe.sub.2 G3 Q229 H NHCOMe G3 Q230 H NO.sub.2 G3 Q246 H NMe.sub.2 G3 Q250 H NO.sub.2 G3 ______________________________________ TABLE 2 ______________________________________ ##STR24## A B D Gn ______________________________________ Q1 H COOMe Gb CH.sub.2 - Q1 H COOMe Gc CHMe - Q1 H COOMe G3 Q2 H COOMe Gb Q3 H COOMe Gb Q4 H COOMe Gb Q5 H COOMe Ga CH.sub.2 - Q5 H COOMe Gc CHMe - Q5 H COOMe G3 Q6 H COOMe G3 Q7 H COOMe G3 Q8 H COOMe G3 Q9 H COOMe Gc CH.sub.2 - Q9 H COOMe Gc Q10 H COOMe Gc Q11 H COOMe G3 Q12 H COOMe G3 Q13 H COOMe G3 Q14 H COOMe G1 Q15 H COOMe G3 Q16 H COOMe Gc Q17 H COOMe Gc Q18 HCOOMe G3 Q19 H COOMe Gc Q20 H COOMe Gc Q21 H COOMe Gc Q22 H COOMe G3 Q23 H COOMe Gc CH.sub.2 - Q23 H COOMe G3 Q24 H COOMe Gc Q25 H COOMe Gb Q26 H COOMe Ga CH.sub.2 - Q26 H COOMe G3 CHMe - Q26 H COOMe G3 Q27 H COOMe G3 Q28 H COOMe G3 Q29 HCOOMe Gc CH.sub.2 - Q29 H COOMe G3 Q30 H COOMe G3 Q31 H COOMe Gc Q32 H COOMe Gc CH.sub.2 - Q32 H COOMe G3 Q33 H COOMe G3 Q34 H COOMe G3 Q35 H COOMe G3 Q36 H COOMe G3 Q37 H COOMe Gc Q38 H COOMe Gc Q39 H COOMe G3 Q40 H COOMe Gc Q41 H COOMeGc Q42 H COOMe Gc Q43 H COOMe G3 Q44 H COOMe Gc Q45 H COOMe Gc Q46 H COOMe Gc Q47 H COOMe Gc Q48 H COOMe Gc Q49 H COOMe G3 Q50 H COOMe Gc CH.sub.2 - Q50 H COOMe G3 Q51 H COOMe Gc Q52 H COOMe G3 Q53 H COOMe G3 Q54 H COOMe Gc Q55 H COOMe Gc Q56 H COOMe Gc Q57 H COOMe G3 Q58 H COOMe Gc Q59 H COOMe Gc CH.sub.2 - Q59 H COOMe G3 Q60 H COOMe Gc Q61 H COOMe Ga CH.sub.2 - Q61 H COOMe Gb CHMe - Q61 H COOMe Gc Q62 H COOMe Gc Q63 H COOMe Gc Q64 H COOMe Gb CH.sub.2 - Q64 H COOMe G3 CHMe - Q64 H COOMe G3 Q65 H COOMe G3 Q66 H COOMe G3 Q67 H COOMe G3 Q68 H COOMe G3 Q69 H COOMe Gc Q70 H COOMe Gc Q71 H COOMe Gc Q72 H COOMe Gc CH.sub.2 - Q72 H COOMe G3 CHMe - Q72 H COOMe G3 Q73 H COOMe Gc CH.sub.2 - Q73 H COOMe G3 Q74 HCOOMe Gc Q75 H COOMe G3 Q76 H COOMe G3 Q77 H COOMe Gc CH.sub.2 - Q77 H COOMe G3 Q78 H COOMe Gc Q79 H COOMe Gc Q80 H COOMe Gc Q81 H COOMe G3 Q82 H COOMe G3 Q83 H COOMe G1 Q84 H COOMe G2 Q85 H COOMe G3 Q86 H COOMe Gc Q87 H COOMe G2 Q88 HCOOMe Gc Q89 H COOMe Gc Q90 H COOMe Gc Q91 H COOMe Gc Q92 H COOMe G3 Q93 H COOMe Gc Q94 H COOMe G3 Q95 H COOMe Gc Q96 H COOMe G3 Q97 H COOMe Gc Q98 H COOMe Gc Q99 H COOMe Gc Q100 H COOMe Gc Q101 H COOMe Gc CH.sub. 2 - Q101 H COOMe G3 Q102H COOMe G3 Q103 H COOMe G3 Q104 H COOMe G3 Q105 H COOMe Gc Q106 H COOMe G3 Q107 H COOMe Gc Q108 H COOMe G1 Q109 H COOMe G3 Q110 H COOMe G3 Q111 H COOMe G3 Q112 H COOMe Gc Q113 H COOMe Gc Q114 H COOMe Gc Q115 H COOMe G2 Q116 H COOMe Gc Q117H COOMe Gc Q118 H COOMe G3 Q119 H COOMe Gc Q120 H COOMe Gc Q121 H COOMe G2 Q122 H COOMe Gc Q123 H COOMe Gc Q124 H COOMe Gc Q125 H COOMe Gc Q126 H COOMe Gc Q127 H COOMe Gc Q128 H COOMe Gc Q129 H COOMe Gc Q130 H COOMe G2 Q131 H COOMe Gc Q132H COOMe Gc Q133 H COOMe G3 Q134 H COOMe G3 Q135 H COOMe Gc Q136 H COOMe G3 Q137 H COOMe G1 Q138 H COOMe Gc CH.sub.2 - Q138 H COOMe G3 Q139 H COOMe G3 Q140 H COOMe G1 Q141 H COOMe G3 Q142 H COOMe Gc Q143 H COOMe Gc CH.sub.2 - Q143 H COOMeG3 Q144 H COOMe G3 Q145 H COOMe Gc Q146 H COOMe Gc Q147 H COOMe G3 Q148 H COOMe G1 Q149 H COOMe G3 Q150 H COOMe G3 Q151 H COOMe G2 Q152 H COOMe G1 Q153 H COOMe Gc Q154 H COOMe Gc Q155 H COOMe G3 Q156 H COOMe G3 Q157 H COOMe Gc Q158 H COOMeGa CH.sub.2 - Q158 H COOMe G3 CHMe - Q158 H COOMe G3 Q159 H COOMe G3 Q160 H COOMe Gc Q161 H COOMe Gc Q162 H COOMe Gc Q163 H COOMe G3 Q164 H COOMe Gc Q165 H COOMe Gc Q166 H COOMe Gc Q167 H COOMe G3 Q168 H COOMe G3 Q169 H COOMe Gc CH.sub.2 -Q169 H COOMe G3 CHMe - Q169 H COOMe G3 Q170 H COOMe Gc Q171 H COOMe Gc Q172 H COOMe Gc Q173 H COOMe Gc Q174 H COOMe Gc Q175 H COOMe Gc Q176 H COOMe Gc Q177 H COOMe Gc CH.sub.2 - Q177 H COOMe G3 CHMe - Q177 H COOMe G3 Q178 H COOMe G3 Q179 HCOOMe G3 Q180 H COOMe Gc CH.sub.2 - Q180 H COOMe G3 Q181 H COOMe G1 Q182 H COOMe G3 Q183 H COOMe G3 Q184 H COOMe Gc CH.sub.2 - Q184 H COOMe G3 CHMe - Q184 H COOMe G3 Q185 H COOMe G3 Q186 H COOMe G3 Q187 H COOMe G3 Q188 H COOMe Gb Q189 HCOOMe Gb Q1 H COOEt Gb CH.sub.2 - Q1 H COOEt Gc CHMe - Q1 H COOEt G3 Q2 H COOEt Gb Q3 H COOEt Gb Q4 H COOEt Gb Q5 H COOEt Ga CH.sub.2 - Q5 H COOEt Gc CHMe - Q5 H COOEt G3 Q6 H COOEt G3 Q7 H COOEt G3 Q8 H COOEt G3 Q9 H COOEt Gc CH.sub.2 - Q9 H COOEt Gc Q10 H COOEt Gc Q11 H COOEtG3 Q12 H COOEt G3 Q13 H COOEt G3 Q14 H COOEt G1 Q15 H COOEt G3 Q16 H COOEt Gc Q17 H COOEt Gc Q18 H COOEt G3 Q19 H COOEt Gc Q20 H COOEt Gc Q21 H COOEt Gc Q22 H COOEt G3 Q23 H COOEt Gc CH.sub.2 - Q23 H COOEt G3 Q24 H COOEt Gc Q25 H COOEt Gb Q26 H COOEt Ga CH.sub.2 - Q26 H COOEt G3 CHMe - Q26 H COOEt G3 Q27 H COOEt G3 Q28 H COOEt G3 Q29 H COOEt Gc CH.sub.2 - Q29 H COOEt G3 Q30 H COOEt G3 Q31 H COOEt Gc Q32 H COOEt Gc CH.sub.2 - Q32 H COOEt G3 Q33 H COOEt G3 Q34 H COOEt G3 Q35H COOEt G3 Q36 H COOEt G3 Q37 H COOEt Gc Q38 H COOEt Gc Q39 H COOEt G3 Q40 H COOEt Gc Q41 H COOEt Gc Q42 H COOEt Gc Q43 H COOEt G3 Q44 H COOEt Gc Q45 H COOEt Gc Q46 H COOEt Gc Q47 H COOEt Gc Q48 H COOEt Gc Q49 H COOEt G3 Q50 H COOEt Gc CH.sub.2 - Q50 H COOEt G3 Q51 H COOEt Gc Q52 H COOEt G3 Q53 H COOEt G3 Q54 H COOEt Gc Q55 H COOEt Gc Q56 H COOEt Gc Q57 H COOEt G3 Q58 H COOEt Gc Q59 H COOEt Gc CH.sub.2 - Q59 H COOEt G3 Q60 H COOEt Gc Q61 H COOEt Ga CH.sub.2 - Q61 HCOOEt Gb CHMe - Q61 H COOEt Gc Q62 H COOEt Gc Q63 H COOEt Gc Q64 H COOEt Gb CH.sub. 2 - Q64 H COOEt G3 CHMe - Q64 H COOEt G3 Q65 H COOEt G3 Q66 H COOEt G3 Q67 H COOEt G3 Q68 H COOEt G3 Q69 H COOEt Gc Q70 H COOEt Gc Q71 H COOEt Gc Q72 HCOOEt Gc CH.sub.2 - Q72 H COOEt G3 CHMe - Q72 H COOEt G3 Q73 H COOEt Gc CH.sub.2 - Q73 H COOEt G3 Q74 H COOEt Gc Q75 H COOEt G3 Q76 H COOEt G3 Q77 H COOEt Gc CH.sub.2 - Q77 H COOEt G3 Q78 H COOEt Gc Q79 H COOEt Gc Q80 H COOEt Gc Q81 HCOOEt G3 Q82 H COOEt G3 Q83 H COOEt G1 Q84 H COOEt G2 Q85 H COOEt G3 Q86 H COOEt Gc Q87 H COOEt G2 Q88 H COOEt Gc Q89 H COOEt Gc Q90 H COOEt Gc Q91 H COOEt Gc Q92 H COOEt G3 Q93 H COOEt Gc Q94 H COOEt G3 Q95 H COOEt Gc Q96 H COOEt G3 Q97H COOEt Gc Q98 H COOEt Gc Q99 H COOEt Gc Q100 H COOEt Gc Q101 H COOEt Gc CH.sub.2 - Q101 H COOEt G3 Q102 H COOEt G3 Q103 H COOEt G3 Q104 H COOEt G3 Q105 H COOEt Gc Q106 H COOEt G3 Q107 H COOEt Gc Q108 H COOEt G1 Q109 H COOEt G3 Q110 HCOOEt G3 Q111 H COOEt G3 Q112 H COOEt Gc Q113 H COOEt Gc Q114 H COOEt Gc Q115 H COOEt G2 Q116 H COOEt Gc Q117 H COOEt Gc Q118 H COOEt G3 Q119 H COOEt Gc Q120 H COOEt Gc Q121 H COOEt G2 Q122 H COOEt Gc Q123 H COOEt Gc Q124 H COOEt Gc Q125 HCOOEt Gc Q126 H COOEt Gc Q127 H COOEt Gc Q128 H COOEt Gc Q129 H COOEt Gc Q130 H COOEt G2 Q131 H COOEt Gc Q132 H COOEt Gc Q133 H COOEt G3 Q134 H COOEt G3 Q135 H COOEt Gc Q136 H COOEt G3 Q137 H COOEt G1 Q138 H COOEt Gc CH.sub.2 - Q138 HCOOEt G3 Q139 H COOEt G3 Q140 H COOEt G1 Q141 H COOEt G3 Q142 H COOEt Gc Q143 H COOEt Gc CH.sub.2 - Q143 H COOEt G3 Q144 H COOEt G3 Q145 H COOEt Gc Q146 H COOEt Gc Q147 H COOEt G3 Q148 H COOEt G1 Q149 H COOEt G3 Q150 H COOEt G3 Q151 HCOOEt G2 Q152 H COOEt G1 Q153 H COOEt Gc Q154 H COOEt Gc Q155 H COOEt G3 Q156 H COOEt G3 Q157 H COOEt Gc Q158 H COOEt Ga CH.sub.2 - Q158 H COOEt G3 CHMe - Q158 H COOEt G3 Q159 H COOEt G3 Q160 H COOEt Gc Q161 H COOEt Gc Q162 H COOEt Gc Q163H COOEt G3 Q164 H COOEt Gc Q165 H COOEt Gc Q166 H COOEt Gc Q167 H COOEt G3 Q168 H COOEt G3 Q169 H COOEt Gc CH.sub.2 - Q169 H COOEt G3 CHMe - Q169 H COOEt G3 Q170 H COOEt Gc Q171 H COOEt Gc Q172 H COOEt Gc Q173 H COOEt Gc Q174 H COOEt Gc Q175 H COOEt Gc Q176 H COOEt Gc Q177 H COOEt Gc CH.sub.2 - Q177 H COOEt G3 CHMe - Q177 H COOEt G3 Q178 H COOEt G3 Q179 H COOEt G3 Q180 H COOEt Gc CH.sub.2 - Q180 H COOEt G3 Q181 H COOEt G1 Q182 H COOEt G3 Q183 H COOEt G3 Q184 H COOEt Gc CH.sub.2 - Q184 H COOEt G3 CHMe - Q184 H COOEt G3 Q185 H COOEt G3 Q186 H COOEt G3 Q187 H COOEt G3 Q188 H COOEt Gb Q189 H COOEt Gb Q5 H COOPri G3 Q26 H COOPri G3 Q61 H COOPri G3 Q158 H COOPri G3 Q5 H COOCH.sub.2 CH.sub.2 Cl G3 Q26 HCOOCH.sub.2 CH.sub.2 Cl G3 Q61 H COOCH.sub.2 CH.sub.2 Cl G3 Q158 H COOCH.sub.2 CH.sub.2 Cl G3 Q5 H COOCH.sub.2 CHCH.sub.2 G3 Q26 H COOCH.sub.2 CHCH.sub.2 G3 Q61 H COOCH.sub.2 CHCH.sub.2 G3 Q158 H COOCH.sub.2 CHCH.sub.2 G3 Q5 H COOCH.sub.2 C CH G3 Q26 H COOCH.sub.2 C CH G3 Q61 H COOCH.sub.2 C CH G3 Q158 H COOCH.sub.2 CCH G3 Q1 H COOPri G3 Q2 H COOCH.sub.2 CH.sub.2 Cl G3 Q4 H COOCH.sub.2 CHCH.sub.2 G3 Q7 H COOCH.sub.2 C CH G3 Q9 H COOPri G3 Q10 H COOCH.sub.2 CH.sub.2 Cl G3 Q19 H COOPri G3 Q23 H COOCH.sub.2 CHCH.sub.2 G3 Q32 H COOCH.sub.2 C CH G3 Q41 HCOOPri G3 Q45 H COOCH.sub.2 CH.sub.2 Cl G3 Q50 H COOCH.sub.2 C CH G3 Q69 H COOPri G3 Q79 H COOCH.sub.2 CH.sub.2 Cl G3 Q83 H COOCH.sub.2 C CH G3 Q96 H COOPri G3 Q124 H COOCH.sub.2 CH.sub.2 Cl G3 Q131 H COOCH.sub.2 CHCH.sub.2 G3 Q132 HCOOCH.sub.2 C CH G3 Q135 H COOPri G3 Q138 H COOPri G3 Q142 H COOCH.sub.2 CHCH.sub.2 G3 Q157 H COOPri G3 Q159 H COOCH.sub.2 CH.sub.2 Cl G3 Q177 H COOCH.sub.2 CHCH.sub.2 G3 Q180 H COOCH.sub.2 C CH G3 Q184 H COOPri G3 Q5 H COOH G3 Q26 H COOHG3 Q61 H COOH G3 Q158 H COOH G3 Q5 H CONHMe G3 Q26 H CONHMe G3 Q61 H CONHMe G3 Q158 H CONHMe G3 Q5 H CONMe.sub.2 G3 Q26 H CONMe.sub.2 G3 Q61 H CONMe.sub.2 G3 Q158 H CONMe.sub.2 G3 Q5 H COMe G3 Q26 H COMe G3 Q61 H COMe G3 Q158 H COMe G3 Q189 H COMe Gb Q5 H COEt G3 Q26 H COEt G3 Q61 H COEt G3 Q158 H COEt G3 Q189 H COEt Gb Q5 H COPri G3 Q26 H COPri G3 Q61 H COPri G3 Q158 H COPri G3 Q5 H COPh G3 Q26 H COPh G3 Q61 H COPh G3 Q158 H COPh G3 Q1 H COMe G3 Q2 H COEt G3 Q4 H COMeG3 Q7 H COMe G3 Q9 H COEt G3 Q10 H COPri G3 Q19 H COPh G3 Q23 H COMe G3 Q32 H COMe G3 Q41 H COPri G3 Q45 H COPh G3 Q50 H COMe G3 Q69 H COEt G3 Q79 H COPri G3 Q83 H COPh G3 Q96 H COMe G3 Q124 H COEt G3 Q131 H COMe G3 Q132 H COMe G3 Q135 HCOEt G3 Q138 H COPri G3 Q142 H COPh G3 Q157 H COMe G3 Q159 H COEt G3 Q177 H COMe G3 Q180 H COMe G3 Q184 H COPri G3 Q4 H CN G3 Q5 H CN G3 Q7 H CN G3 Q9 H CN G3 Q23 H CN G3 Q26 H CN G3 Q32 H CN G3 Q61 H CN G3 Q96 H CN G3 Q142 H CN G3 Q158H CN G3 Q5 H H G3 Q26 H H G3 Q61 H H G3 Q158 H H G3 Q5 H Me G3 Q26 H Me G3 Q61 H Me G3 Q158 H Me G3 Q5 H Et G3 Q26 H Et G3 Q61 H Et G3 Q158 H Et G3 Q5 H Pri G3 Q26 H Pri G3 Q61 H Pri G3 Q158 H Pri G3 Q5 H CHCH.sub.2 G3 Q26 H CHCH.sub.2G3 Q61 H CHCHMe G3 Q158 H CHCHMe G3 Q5 H CH.sub.2 CHCH.sub.2 G3 Q26 H CH.sub.2 CHCH.sub.2 G3 Q61 H CH.sub.2 CHCH.sub. 2 G3 Q158 H CH.sub.2 CHCH.sub.2 G3 Q1 H H G3 Q2 H Me G3 Q4 H Me G3 Q7 H Me G3 Q9 H Et G3 Q10 H Pri G3 Q19 H Me G3 Q23H CH.sub.2 CHCH.sub.2 G3 Q32 H H G3 Q41 H Me G3 Q45 H Me G3 Q50 H Et G3 Q69 H Pri G3 Q79 H Me G3 Q83 H Et G3 Q96 H Me G3 Q124 H Et G3 Q131 H Me G3 Q132 H CH.sub.2 CHCH.sub.2 G3 Q135 H Et G3 Q138 H Pri G3 Q142 H H G3 Q157 H Me G3 Q159 HMe G3 Q177 H H G3 Q180 H Me G3 Q184 H Me G3 Q5 H CH.sub.2 Cl G3 Q26 H CH.sub.2 Cl G3 Q61 H CH.sub.2 Cl G3 Q158 H CH.sub.2 Cl G3 Q5 H CH.sub.2 CH.sub.2 Cl G3 Q26 H CH.sub.2 CH.sub.2 Cl G3 Q61 H CH.sub.2 CH.sub.2 Cl G3 Q158 H CH.sub.2CH.sub.2 Cl G3 Q5 H CF.sub.3 G3 Q26 H CF.sub.3 G3 Q61 H CF.sub.3 G3 Q158 H CF.sub.3 G3 Q5 H CFCFCl G3 Q26 H CFCFCl G3 Q61 H CH.sub.2 Ph G3 Q158 H CH.sub.2 Ph G3 Q5 H Ph G3 Q26 H Ph G3 Q61 H Ph G3 Q158 H Ph G3 Q5 H Ph2-Cl G3 Q26 H Ph2-Me G3 Q61 H Ph2-Cl G3 Q158 H Ph2-Me G3 Q1 H Ph G3 Q2 H CH.sub.2 Cl G3 Q4 H CH.sub.2 CH.sub.2 Cl G3 Q7 H Ph G3 Q9 H CF.sub.3 G3 Q10 H CF.sub.3 G3 Q19 H CFCFCl G3 Q23 H CH.sub.2 CH.sub.2 Cl G3 Q32 H Ph G3 Q41 H Ph2-Cl G3 Q45 H Ph2-Me G3 Q50 HCH.sub.2 CH.sub.2 Cl G3 Q69 H Ph G3 Q79 H CF.sub.3 G3 Q83 H CF.sub.3 G3 Q96 H Ph G3 Q124 H Ph2-Cl G3 Q131 H Ph2-Me G3 Q132 H CH.sub.2 CH.sub.2 Cl G3 Q135 H Ph G3 Q138 H CF.sub.3 G3 Q142 H CF.sub.3 G3 Q157 H CFCFCl G3 Q159 H CH.sub.2 Cl G3 Q177 H CH.sub.2 CH.sub.2 Cl G3 Q180 H Ph G3 Q184 H Ph2-Cl G3 Q5 H Cl G3 Q26 H Cl G3 Q61 H Cl G3 Q158 H Cl G3 Q5 H Br G3 Q26 H Br G3 Q61 H Br G3 Q158 H Br G3 Q5 H F G3 Q26 H F G3 Q61 H I G3 Q158 H I G3 Q1 H Cl G3 Q2 H Cl G3 Q4 H Cl G3 Q7 H Br G3 Q9 H F G3 Q10 H I G3 Q19 H Cl G3 Q23 H Cl G3 Q32 H Cl G3 Q41 H Br G3 Q45 H Br G3 Q50 H F G3 Q69 H ClG3 Q79 H F G3 Q83 H Cl G3 Q96 H Cl G3 Q124 H Cl G3 Q131 H Br G3 Q132 H Br G3 Q135 H F G3 Q138 H Br G3 Q142 H Cl G3 Q157 H Cl G3 Q159 H Cl G3 Q177 H Br G3 Q180 H Br G3 Q184 H Cl G3 Q4 H NO.sub.2 G3 Q5 H NO.sub.2 G3 Q7 H NO.sub.2 G3 Q9 HNO.sub.2 G3 Q23 H NO.sub.2 G3 Q26 H NO.sub.2 G3 Q32 H NO.sub.2 G3 Q61 H NO.sub.2 G3 Q96 H NO.sub.2 G3 Q142 H NO.sub.2 G3 Q158 H NO.sub.2 G3 Q5 H NH.sub.2 G3 Q26 H NH.sub.2 G3 Q61 H NH.sub.2 G3 Q158 H NH.sub.2 G3 Q5 H NHMe G3 Q26 H NHMe G3 Q61 H NHMe G3 Q158 H NHMe G3 Q5 H NMe.sub.2 G3 Q26 H NMe.sub.2 G3 Q61 H NMe.sub.2 G3 Q158 H NMe.sub.2 G3 Q5 H NMeEt G3 Q26 H NMeEt G3 Q61 H NMeEt G3 Q158 H NMeEt G3 Q5 H NHSO.sub.2 Me G3 Q26 H NHSO.sub.2 Me G3 Q61 H NHSO.sub.2 Me G3 Q158 HNHSO.sub.2 Me G3 Q1 H NH.sub.2 G3 Q2 H NH.sub.2 G3 Q4 H NH.sub.2 G3 Q7 H NHMe G3 Q9 H NHMe G3 Q10 H NMe.sub.2 G3 Q19 H NMeEt G3 Q23 H NMe.sub.2 G3 Q32 H NMeEt G3 Q41 H NH.sub.2 G3 Q45 H NH.sub.2 G3 Q50 H NHMe G3 Q69 H NHMe G3 Q79 HNMe.sub.2 G3 Q83 H NMeEt G3 Q96 H NHSO.sub.2 Me G3 Q124 H NMe.sub.2 G3 Q131 H NMeEt G3 Q132 H NH.sub.2 G3 Q135 H NH.sub.2 G3 Q138 H NHMe G3 Q142 H NHMe G3 Q157 H NHSO.sub.2 Me G3 Q159 H NMe.sub.2 G3 Q177 H NMeEt G3 Q180 H NH.sub.2 G3 Q184 HNH.sub.2 G3 Q4 H NHCOMe G3 Q5 H NHCOMe G3 Q7 H NHCOMe G3 Q9 H NHCOMe G3 Q23 H NHCOMe G3 Q26 H NHCOMe G3 Q32 H NHCOMe G3 Q61 H NHCOMe G3 Q96 H NHCOMe G3 Q142 H NHCOMe G3 Q158 H NHCOMe G3 Q5 H NHCOEt G3 Q26 H NHCOEt G3 Q61 H NHCOEt G3 Q158 H NHCOEt G3 Q5 H OMe G3 Q26 H OMe G3 Q61 H OMe G3 Q158 H OMe G3 Q5 H OEt G3 Q26 H OEt G3 Q61 H OEt G3 Q158 H OEt G3 Q5 H CH.sub.2OMe G3 Q26 H CH.sub.2 OMe G3 Q61 H CH.sub.2 OMe G3 Q158 H CH.sub.2 OMe G3 Q5 H SMe G3 Q26 H SMe G3 Q61 H SMe G3 Q158 H SMe G3 Q5 H SO.sub.2 OMe G3 Q26 H SO.sub.2 OMe G3 Q61 H SO.sub.2 OMe G3 Q158 H SO.sub.2 OMe G3 Q1 H OMe G3 Q2 H OMe G3 Q4H OEt G3 Q7 H SO.sub.2 OMe G3 Q9 H CH.sub.2 OMe G3 Q10 H SMe G3 Q19 H SO.sub.2 OMe G3 Q23 H OMe G3 Q32 H OEt G3 Q41 H SO.sub.2 OMe G3 Q45 H CH.sub.2 OMe G3 Q50 H SMe G3 Q69 H SO.sub.2 OMe G3 Q79 H OMe G3 Q83 H OEt G3 Q96 H CH.sub.2 OMe G3 Q124 H SMe G3 Q131 H OMe G3 Q132 H OEt G3 Q135 H CH.sub.2 OMe G3 Q138 H SMe G3 Q142 H SO.sub.2 OMe G3 Q157 H OMe G3 Q159 H OEt G3 Q177 H SO.sub.2 OMe G3 Q180 H OMe G3 Q184 H OEt G3 Q4 H SO.sub.2 Me G3 Q5 H SO.sub.2 Me G3 Q7 H SO.sub.2 Me G3 Q9 H SO.sub.2 Me G3 Q23 H SO.sub.2 Me G3 Q26 H SO.sub.2 Me G3 Q32 H SO.sub.2 Me G3 Q61 H SO.sub.2 Me G3 Q96 H SO.sub.2 Me G3 Q142 H SO.sub.2 Me G3 Q158 H SO.sub.2 Me G3 Q188 H SO.sub.2 Me Gb Q189 H SO.sub. 2 Me Gb Q5 H SO.sub.2 Ph G3 Q26 HSO.sub.2 Ph G3 Q61 H SO.sub.2 Ph G3 Q158 H SO.sub.2 Ph G3 Q5 H SO.sub.2 NH.sub.2 G3 Q26 H SO.sub.2 NH.sub.2 G3 Q61 H SO.sub.2 NH.sub.2 G3 Q158 H SO.sub.2 NH.sub.2 G3 Q5 H SO.sub.2 NHMe G3 Q26 H SO.sub.2 NHMe G3 Q61 H SO.sub.2 NHMe G3 Q158 HSO.sub.2 NHMe G3 Q5 H SO.sub.2 NMe.sub.2 G3 Q26 H SO.sub.2 NMe.sub.2 G3 Q61 H SO.sub.2 NMe.sub.2 G3 Q158 H SO.sub.2 NMe.sub.2 G3 Q1 H SO.sub.2 Me G3 Q2 H SO.sub.2 Me G3 Q4 H SO.sub.2 Ph G3 Q7 H SO.sub.2 NH.sub.2 G3 Q9 H SO.sub.2 NH.sub.2 G3 Q10 H SO.sub.2 Ph G3 Q19 H SO.sub.2 Me G3 Q23 H SO.sub.2 Ph G3 Q32 H SO.sub.2 NHMe G3 Q41 H SO.sub.2 NMe.sub.2 G3 Q45 H SO.sub.2 Me G3 Q50 H SO.sub.2 NH.sub.2 G3 Q69 H SO.sub.2 Me G3 Q79 H SO.sub.2 Ph G3 Q83 H SO.sub.2 Me G3 Q96 HSO.sub.2 NMe.sub.2 G3 Q124 H SO.sub.2 NH.sub.2 G3 Q131 H SO.sub.2 Me G3 Q132 H SO.sub.2 Me G3 Q135 H SO.sub.2 NHMe G3 Q138 H SO.sub.2 NMe.sub.2 G3 Q142 H SO.sub.2 NH.sub.2 G3 Q157 H SO.sub.2 Me G3 Q159 H SO.sub.2 Me G3 Q177 H SO.sub.2 NHMeG3 Q180 H SO.sub.2 NHMe.sub.2 G3 Q184 H SO.sub.2 Me G3 Q1 Me COOMe G3 Q2 Me COOMe G3 Q4 Me COOMe G3 Q5 Me COOMe G3 Q7 Me COOMe G3 Q9 Me COOMe G3 Q10 Me COOMe G3 Q19 Me COOMe G3 Q23 Me COOMe G3 Q26 Me COOMe G3 Q32 Me COOMe G3 Q41 Me COOMeG3 Q45 Me COOMe G3 Q50 Me COOMe G3 Q61 Me COOMe G3 Q69 Me COOMe G3 Q79 Me COOMe G3 Q83 Me COOMe G3 Q96 Me COOMe G3 Q124 Me COOMe G3 Q131 Me COOMe G3 Q132 Me COOMe G3 Q135 Me COOMe G3 Q138 Me COOMe G3 Q142 Me COOMe G3 Q157 Me COOMe G3 Q158Me COOMe G3 Q159 Me COOMe G3 Q177 Me COOMe G3 Q180 Me COOMe G3 Q184 Me COOMe G3 Q1 Me COOEt G3 Q2 Me COOEt G3 Q4 Me COOEt G3 Q5 Me COOEt G3 Q7 Me COOEt G3 Q9 Me COOEt G3 Q10 Me COOEt G3 Q19 Me COOEt G3 Q23 Me COOEt G3 Q26 Me COOEt G3 Q32Me COOEt G3 Q41 Me COOEt G3 Q45 Me COOEt G3 Q50 Me COOEt G3 Q61 H COOEt G3 Q69 Me COOEt G3 Q79 Me COOEt G3 Q83 Me COOEt G3 Q96 Me COOEt G3 Q124 Me COOEt G3 Q131 Me COOEt G3 Q132 Me COOEt G3 Q135 Me COOEt G3 Q138 Me COOEt G3 Q142 Me COOEt G3 Q157 Me COOEt G3 Q158 Me COOEt G3 Q159 Me COOEt G3 Q177 Me COOEt G3 Q180 Me COOEt G3 Q184 Me COOEt G3 Q158 Me COOEt G3 Q5 Me COOPri G3 Q26 Me COOPri G3 Q61 Me COOPri G3 Q158 Me COOPri G3 Q5 Me COOCH.sub.2 CH.sub.2 Cl G3 Q26 Me COOCH.sub.2CH.sub.2 Cl G3 Q61 Me COOCH.sub.2 CH.sub.2 Cl G3 Q158 Me COOCH.sub.2 CH.sub.2 Cl G3 Q5 Me COOCH.sub.2 CHCH.sub.2 G3 Q26 Me COOCH.sub.2 CHCH.sub.2 G3 Q61 Me COOCH.sub.2 CHCH.sub.2 G3 Q158 Me COOCH.sub.2 CHCH.sub.2 G3 Q5 Me COOCH.sub.2 C CH G3 Q26 Me COOCH.sub.2 C CH G3 Q61 Me COOCH.sub.2 C CH G3 Q158 Me COOCH.sub.2 C CH G3 Q5 Me CONHMe G3 Q26 Me CONHMe G3 Q61 Me CONHMe G3 Q158 Me CONHMe G3 Q5 Me CONMe.sub.2 G3 Q26 Me CONMe.sub.2 G3 Q61 Me CONMe.sub.2 G3 Q158 Me CONMe.sub.2 G3 Q1 Me COOPri G3 Q2 Me COOPri G3 Q4 Me COOCH.sub.2 CH.sub.2 Cl G3 Q7 Me COOCH.sub.2 CHCH.sub.2 G3 Q9 Me COOCH.sub.2 C CH G3 Q10 Me COOCH.sub.2 CH.sub.2 Cl G3 Q19 Me COOPri G3 Q23 Me COOCH.sub.2 CH.sub.2 Cl G3 Q32 Me CONMe.sub.2 G3 Q41 MeCOOPri G3 Q45 Me CONHMe G3 Q50 Me CONMe.sub.2 G3 Q69 Me COOCH.sub.2 CH.sub.2 Cl G3 Q79 Me COOCH.sub.2 CHCH.sub.2 G3 Q83 Me COOPri G3 Q96 Me COOCH.sub.2 CH.sub.2 Cl G3 Q124 Me COOPri G3 Q131 Me COOCH.sub.2 CH.sub.2 Cl G3 Q132 Me CONHMe G3 Q135 Me CONMe.sub.2 G3 Q138 Me COOCH.sub.2 C CH G3 Q142 Me COOPri G3 Q157 Me COOPri G3 Q159 Me COOCH.sub.2 CHCH.sub.2 G3 Q177 Me COOCH.sub.2 C CH G3 Q180 Me COOPri G3 Q184 MeCOOCH.sub.2 CH.sub.2 Cl G3 Q5 Me COMe G3 Q26 Me COMe G3 Q61 Me COMe G3 Q158 Me COMe G3 Q5 Me COEt G3 Q26 Me COEt G3 Q61 Me COEt G3 Q158 Me COEt G3 Q5 Me COPri G3 Q26 Me COPri G3 Q61 Me COPri G3 Q158 Me COPri G3 Q5 Me CN G3 Q26 Me CN G3 Q61 Me CN G3 Q158 Me CN G3 Q5 Me H G3 Q26 Me H G3 Q61 Me H G3 Q158 Me H G3 Q5 Me Me G3 Q26 Me Me G3 Q61 Me Me G3 Q158 Me Me G3 Q5 Me Et G3 Q26 Me Et G3 Q61 Me Et G3 Q158 Me Et G3 Q5 Me Pri G3 Q26 Me Pri G3 Q61 Me CHCH.sub.2 G3 Q158 MeCHCH.sub.2 G3 Q5 Me CHCHMe G3 Q26 Me CH.sub.2 CHCH.sub.2 G3 Q61 Me CHCHMe G3 Q158 Me CH.sub.2 CHCH.sub.2 G3 Q1 Me COMe G3 Q2 Me COEt G3 Q4 Me CHCHMe G3 Q7 Me CH.sub.2 CHCH.sub.2 G3 Q9 Me CN G3 Q10 Me H G3 Q19 Me Me G3 Q23 Me COMe G3 Q32Me COEt G3 Q41 Me H G3 Q45 Me Me G3 Q50 Me COPri G3 Q69 Me CN G3 Q79 Me Et G3 Q83 Me Pri G3 Q96 Me COMe G3 Q124 Me COEt G3 Q131 Me CH.sub.2 CHCH.sub.2 G3 Q132 Me Me G3 Q135 Me COPr-i G3 Q138 Me CN G3 Q142 Me Et G3 Q157 Me CH.sub.2CHCH.sub.2 G3 Q159 Me COMe G3 Q177 Me COEt G3 Q180 Me CHCHMe G3 Q184 Me COMe G3 Q5 Me CH.sub.2 Cl G3 Q26 Me CH.sub. 2 Cl G3 Q5 Me CH.sub.2 CH.sub.2 Cl G3 Q26 Me CH.sub.2 CH.sub.2 Cl G3 Q61 Me CH.sub.2 CH.sub.2 Cl G3 Q158 Me CH.sub.2CH.sub.2 Cl G3 Q5 Me CF.sub.3 G3 Q26 Me CF.sub.3 G3 Q61 Me CF.sub.3 G3 Q158 Me CF.sub.3 G3 Q5 Me CFCFCl G3 Q26 Me CFCFCl G3 Q61 Me CH.sub.2 Ph G3 Q158 Me CH.sub.2 Ph G3 Q5 Me Ph G3 Q26 Me Ph G3 Q61 Me Ph G3 Q158 Me Ph G3 Q5 Me Ph2-Cl G3 Q26 Me Ph2-Cl G3 Q61 Me Ph2-Me G3 Q158 Me Ph2-Me G3 Q5 Me Cl G3 Q26 Me Cl G3 Q61 Me Cl G3 Q158 Me Cl G3 Q5 Me Br G3 Q26 Me Br G3 Q61 Me Br G3 Q158 Me Br G3 Q5 Me F G3 Q26 Me F G3 Q61 Me I G3 Q158 Me I G3 Q1 Me Ph G3 Q2 Me Cl G3 Q4 MeCH.sub.2 CH.sub.2 Cl G3 Q7 Me Ph G3 Q9 Me Ph G3 Q10 Me Cl G3 Q19 Me Cl G3 Q23 Me Br G3 Q32 Me CH.sub. 2 Cl G3 Q41 Me CH.sub.2 CH.sub.2 Cl G3 Q45 Me CF.sub.3 G3 Q50 Me Cl G3 Q69 Me Cl G3 Q79 Me Br G3 Q83 Me Ph G3 Q96 Me CF.sub.3 G3 Q124 MeCF.sub.3 G3 Q131 Me CH.sub.2 CH.sub.2 Cl G3 Q132 Me Ph G3 Q135 Me Br G3 Q138 Me Ph G3 Q142 Me Ph G3 Q157 Me Cl G3 Q159 Me Br G3 Q177 Me CF.sub.3 G3 Q180 Me CH.sub.2 CH.sub.2 Cl G3 Q184 Me Ph G3 Q5 Me NO.sub.2 G3 Q26 Me NO.sub.2 G3 Q61 MeNO.sub.2 G3 Q158 Me NO.sub.2 G3 Q5 Me NH.sub.2 G3 Q26 Me NH.sub.2 G3 Q61 Me NH.sub.2 G3 Q158 Me NH.sub.2 G3 Q5 Me NHMe G3 Q26 Me NHMe G3 Q61 Me NHMe G3 Q158 Me NHMe G3 Q5 Me NMe.sub.2 G3 Q26 Me NMe.sub.2 G3 Q61 Me NMe.sub.2 G3 Q158 MeNMe.sub.2 G3 Q5 Me NMeEt G3 Q26 Me NMeEt G3 Q5 Me NHCOMe G3 Q26 Me NHCOMe G3 Q61 Me NHCOMe G3 Q158 Me NHCOMe G3 Q5 Me NHCOEt G3 Q26 Me NHCOEt G3 Q61 Me NHSO.sub.2 Me G3 Q158 Me NHSO.sub.2 Me G3 Q5 Me OMe G3 Q26 Me OMe G3 Q61 Me OMe G3 Q158Me OMe G3 Q5 Me OEt G3 Q26 Me OEt G3 Q61 Me CH.sub.2 OMe G3 Q158 Me CH.sub.2 OMe G3 Q1 Me NO.sub.2 G3 Q2 Me NHCOMe G3 Q4 Me NHCOEt G3 Q7 Me NHMe G3 Q9 Me NO.sub.2 G3 Q10 Me NH.sub.2 G3 Q19 Me NHCOMe G3 Q23 Me OMe G3 Q32 Me NHCOMe G3 Q41 MeNHCOEt G3 Q45 Me CH.sub.2 OMe G3 Q50 Me OMe G3 Q69 Me OEt G3 Q79 Me NO.sub.2 G3 Q83 Me NH.sub.2 G3 Q96 Me NMe.sub.2 G3 Q124 Me NMeEt G3 Q131 Me NHCOMe G3 Q132 Me NHCOEt G3 Q135 Me NO.sub.2 G3 Q138 Me OMe G3 Q142 Me OEt G3 Q157 Me NO.sub.2 G3 Q159 Me NH.sub.2 G3 Q177 Me OMe G3 Q180 Me NHCOMe G3 Q184 Me NO.sub.2 G3 Q26 Me SMe G3 Q61 Me SMe G3 Q5 Me SO.sub.2 Me G3 Q26 Me SO.sub.2 Me G3 Q61 Me SO.sub.2 Me G3 Q158 Me SO.sub.2 Me G3 Q5 Me SO.sub.2 Ph G3 Q26 Me SO.sub.2 Ph G3 Q61 MeSO.sub.2 Ph G3 Q158 Me SO.sub.2 Ph G3 Q5 Me SO.sub.2 OMe G3 Q26 Me SO.sub.2 OMe G3 Q61 Me SO.sub.2 NH.sub.2 G3 Q158 Me SO.sub.2 NH.sub.2 G3 Q5 Me SO.sub.2 NHMe G3 Q26 Me SO.sub.2 NHMe G3 Q61 Me SO.sub.2 NHMe G3 Q158 Me SO.sub.2 NHMe G3 Q5 MeSO.sub.2 NMe.sub.2 G3 Q26 Me SO.sub.2 NMe.sub.2 G3 Q61 Me SO.sub.2 NMe.sub.2 G3 Q158 Me SO.sub.2 NMe.sub.2 G3 Q1 Me SO.sub.2 Ph G3 Q2 Me SO.sub.2 OMe G3 Q4 Me SO.sub.2 NHMe G3 Q7 Me SO.sub.2 NMe.sub.2 G3 Q9 Me SO.sub.2 Me G3 Q10 Me SO.sub.2Me G3 Q19 Me SMe G3 Q23 Me SO.sub.2 Me G3 Q32 Me SO.sub.2 OMe G3 Q41 Me SO.sub.2 NMe.sub.2 G3 Q45 Me SO.sub.2 NHMe G3 Q50 Me SO.sub.2 NMe.sub.2 G3 Q69 Me SO.sub.2 Me G3 Q79 Me SO.sub.2 Me G3 Q83 Me SO.sub.2 Ph G3 Q96 Me SO.sub.2 OMe G3 Q124 Me SO.sub.2 NMe.sub.2 G3 Q131 Me SO.sub.2 NHMe G3 Q132 MeSO.sub.2 NMe.sub.2 G3 Q135 Me SO.sub.2 Ph G3 Q138 Me SO.sub.2 Ph G3 Q142 Me SO.sub.2 Me G3 Q157 Me SO.sub.2 Me G3 Q159 Me SO.sub.2 NHMe G3 Q177 Me SO.sub.2 NMe.sub.2 G3 Q180 Me SO.sub.2 NMe.sub.2 G3 Q184 Me SO.sub.2 Me.sub.2 G3 Q5 Et COOMeG3 Q26 Et COOMe G3 Q61 Et COOMe G3 Q142 Et COOMe G3 Q158 Et COOMe G3 Q159 Et COOMe G3 Q4 Et COOEt G3 Q5 Et COOEt G3 Q9 Et COOEt G3 Q26 Et COOEt G3 Q32 Et COOEt G3 Q61 Et COOEt G3 Q69 Et COOEt G3 Q96 Et COOEt G3 Q158 Et COOEt G3 Q61 EtCOOPri G3 Q158 Et COOPri G3 Q5 Et COOCH.sub.2 CH.sub.2 Cl G3 Q26 Et COOCH.sub.2 CH.sub.2 Cl G3 Q5 Et COOCH.sub.2 CHCH.sub.2 G3 Q158 Et COOCH.sub.2 CHCH.sub.2 G3 Q5 Et COOCH.sub.2 C CH G3 Q26 Et COOCH.sub.2 C CH G3 Q5 Et CONHMe G3 Q26 EtCONMe.sub.2 G3 Q1 Et COOPri G3 Q4 Et COOCH.sub.2 CH.sub.2 Cl G3 Q69 Et COOCH.sub.2 CH.sub.2 Cl G3 Q79 Et COOCH.sub.2 CHCH.sub.2 G3 Q83 Et COOPri G3 Q96 Et COOCH.sub.2 CH.sub.2 Cl G3 Q131 Et COOCH.sub.2 CH.sub.2 Cl G3 Q157 Et COOPri G3 Q159Et COOCH.sub.2 CHCH.sub.2 G3 Q184 Et COOCH.sub.2 CH.sub.2 Cl G3 Q5 Et COMe G3 Q26 Et COMe G3 Q158 Et COEt G3 Q5 Et COPri G3 Q26 Et CN G3 Q61 Et H G3 Q26 Et Me G3 Q158 Et Et G3 Q5 Et Pri G3 Q1 Et COMe G3 Q2 Et COEt G3 Q9 Et CN G3 Q23 EtCOMe G3 Q96 Et COMe G3 Q124 Et COEt G3 Q135 Et COPri G3 Q138 Et CN G3 Q5 Et CH.sub.2 CH.sub.2 Cl G3 Q26 Et CH.sub.2 CH.sub.2 Cl G3 Q158 Et CF.sub.3 G3 Q5 Et Ph G3 Q26 Et Ph G3 Q158 Et Ph2-Me G3 Q26 Et Cl G3 Q61 Et Cl G3 Q5 Et Br G3 Q1 EtPh G3 Q2 Et Cl G3 Q9 Et Ph G3 Q5 Et NO.sub.2 G3 Q5 Et NH.sub.2 G3 Q5 Et NHMe G3 Q26 Et NMe.sub.2 G3 Q61 Et NHCOMe G3 Q158 Et NHSO.sub.2 Me G3 Q2 Et NHCOMe G3 Q23 Et OMe G3 Q32 Et NHCOMe G3 Q96 Et NMe.sub.2 G3 Q26 Et SO.sub.2 Me G3 Q61 EtSO.sub.2 Me G3 Q5 Et SO.sub.2 Ph G3 Q26 Et SO.sub.2 OMe G3 Q61 Et SO.sub.2 NH.sub.2 G3 Q5 Et SO.sub.2 NHMe G3 Q26 Et SO.sub.2 NMe.sub.2 G3 Q4 Et SO.sub.2 NHMe G3 Q7 Et SO.sub.2 NMe.sub.2 G3 Q9 Et SO.sub.2 Me G3 Q142 Et SO.sub.2 Me G3 Q159 EtSO.sub.2 NMe.sub.2 G3 Q5 Cl COOMe G3 Q26 Cl COOMe G3 Q61 Cl COOMe G3 Q5 Cl COOEt G3 Q26 Cl COOEt G3 Q61 Cl COOEt G3 Q96 Cl COOEt G3 Q158 Cl COOEt G3 Q61 Cl COOPri G3 Q5 Cl COMe G3 Q158 Cl COEt G3 Q5 Cl COPri G3 Q26 Cl CN G3 Q61 Cl H G3 Q26 Cl Me G3 Q158 Cl Et G3 Q5 Cl Pri G3 Q1 Cl COMe G3 Q26 Cl CH.sub.2 CH.sub.2 Cl G3 Q158 Cl CF.sub.3 G3 Q5 Cl Ph G3 Q26 Cl Cl G3 Q5 Cl Br G3 Q2 Cl Cl G3 Q9 Cl Ph G3 Q5 Cl NO.sub.2 G3 Q5 Cl NH.sub.2 G3 Q5 Cl NHMe G3 Q26 Cl NMe.sub.2 G3 Q61 Cl NHCOMe G3 Q158 Cl NHSO.sub.2 Me G3 Q2 Cl NHCOMe G3 Q26 Cl SO.sub.2 Me G3 Q61 Cl SO.sub.2 Me G3 Q5 Cl SO.sub.2 Ph G3 Q61 Cl SO.sub.2 NH.sub.2 G3 Q5 Cl SO.sub.2 NHMe G3 Q26 Cl SO.sub.2 NMe.sub.2 G3 Q5 Br COOMe G3 Q26 Br COOMe G3 Q61 BrCOOMe G3 Q5 Br COOEt G3 Q26 Br COOEt G3 Q61 Br COOEt G3 Q61 Br COOPri G3 Q5 Br COMe G3 Q158 Br COEt G3 Q26 Br CN G3 Q26 Br Me G3 Q158 Br Et G3 Q26 Br CH.sub.2 CH.sub.2 Cl G3 Q158 Br CF.sub.3 G3 Q5 Br Ph G3 Q26 Br Cl G3 Q5 Br Br G3 Q5 BrNO.sub.2 G3 Q5 Br NH.sub.2 G3 Q26 Br NMe.sub.2 G3 Q61 Br NHCOMe G3 Q61 Br SO.sub.2 Me G3 Q5 Br SO.sub.2 Ph G3 Q61 Br SO.sub.2 NH.sub.2 G3 Q26 Br SO.sub.2 NMe.sub.2 G3 Q5 SMe COOMe G3 Q26 SMe COOMe G3 Q61 SMe COOMe G3 Q5 SMe COOEt G3 Q26 SMeCOOEt G3 Q61 SMe COOEt G3 Q61 SMe COOPri G3 Q5 SMe COMe G3 Q158 SMe COEt G3 Q26 SMe CN G3 Q26 SMe Me G3 Q158 SMe Et G3 Q26 SMe CH.sub.2 CH.sub.2 Cl G3 Q158 SMe CF.sub.3 G3 Q5 SMe Ph G3 Q26 SMe Cl G3 Q5 SMe Br G3 Q5 SMe NO.sub.2 G3 Q5 SMeNH.sub.2 G3 Q26 SMe NMe.sub.2 G3 Q61 SMe NHCOMe G3 Q61 SMe SO.sub.2 Me G3 Q5 SMe SO.sub.2 Ph G3 Q61 SMe SO.sub.2 NH.sub.2 G3 Q26 SMe SO.sub.2 NMe.sub.2 G3 Q5 SO.sub.2 Me COOMe G3 Q26 SO.sub.2 Me COOMe G3 Q61 SO.sub.2 Me COOMe G3 Q5SO.sub.2 Me COOEt G3 Q26 SO.sub.2 Me COOEt G3 Q61 SO.sub.2 Me COOEt G3 Q96 SO.sub.2 Me COOEt G3 Q158 SO.sub.2 Me COOEt G3 Q61 SO.sub.2 Me COOPr i G3 Q5 SO.sub.2 Me COMe G3 Q158 SO.sub.2 Me COEt G3 Q5 SO.sub.2 Me COPri G3 Q26 SO.sub.2 Me CN G3 Q61 SO.sub.2 Me H G3 Q26 SO.sub.2 Me Me G3 Q158 SO.sub.2 Me Et G3 Q5 SO.sub.2 Me Pri G3 Q1 SO.sub.2 Me COMe G3 Q26 SO.sub.2 Me CH.sub.2 CH.sub.2 Cl G3 Q158 SO.sub.2 Me CF.sub.3 G3 Q5 SO.sub.2 Me Ph G3 Q26SO.sub.2 Me Cl G3 Q5 SO.sub.2 Me Br G3 Q2 SO.sub.2 Me Cl G3 Q9 SO.sub.2 Me Ph G3 Q5 SO.sub.2 Me NO.sub.2 G3 Q5 SO.sub.2 Me NH.sub.2 G3 Q5 SO.sub.2 Me NHMe G3 Q26 SO.sub.2 Me NMe.sub.2 G3 Q61 SO.sub.2 Me NHCOMe G3 Q158 SO.sub.2 Me NHSO.sub.2 Me G3 Q2 SO.sub.2 Me NHCOMe G3 Q26 SO.sub.2 Me SO.sub.2 Me G3 Q61 SO.sub.2 Me SO.sub.2 Me G3 Q5 SO.sub.2 Me SO.sub.2 Ph G3 Q61 SO.sub.2 Me SO.sub.2 NH.sub.2 G3 Q5 SO.sub.2 Me SO.sub.2 NHMe G3 Q26 SO.sub.2 Me SO.sub.2 NMe.sub. 2 G3 Q5 Ph COOMe G3 Q26 Ph COOMe G3 Q61 Ph COOMe G3 Q5 Ph COOEt G3 Q26 Ph COOEt G3 Q61 Ph COOEt G3 Q61 Ph COOPri G3 Q5 Ph COMe G3 Q158 Ph COEt G3 Q26 Ph CN G3 Q26 Ph Me G3 Q158 Ph Et G3 Q26 Ph CH.sub.2 CH.sub.2 Cl G3 Q158 Ph CF.sub.3 G3 Q5Ph Ph G3 Q26 Ph Cl G3 Q5 Ph Br G3 Q5 Ph NO.sub.2 G3 Q5 Ph NH.sub.2 G3 Q26 Ph NMe.sub.2 G3 Q61 Ph NHCOMe G3 Q61 Ph SO.sub.2 Me G3 Q5 Ph SO.sub.2 Ph G3 Q61 Ph SO.sub.2 NH.sub.2 G3 Q26 Ph SO.sub.2 NMe.sub.2 G3 Q201 H COOMe Ga CH.sub.2 - Q201 H COOMe Gb CHMe - Q201 H COOMe Gb Q202 H COOMe Gb CH.sub.2 - Q202 H COOMe Gb Q203 H COOMe Gb Q204 H COOMe Gb Q205 H COOMe Gb CH.sub.2 - Q205 H COOMe Gc Q206 H COOMe G.sub.3 Q207 H COOMe Gc Q208 H COOMe G.sub.3 Q209 H COOMe Gc CH.sub.2 -Q209 H COOMe Gc Q210 H COOMe Gc CH.sub.2 - Q210 H COOMe G.sub.3 Q211 H COOMe G.sub.3 Q212 H COOMe Gc Q213 H COOMe Gc Q214 H COOMe Gc Q215 H COOMe G.sub.1 Q216 H COOMe Gc Q217 H COOMe Gc Q218 H COOMe G.sub.3 Q219 H COOMe Gc Q220 H COOMe Gc Q221 HCOOMe G.sub.2 Q222 H COOMe Gb CH.sub.2 - Q222 H COOMe Gc Q223 H COOMe Gc Q224 H COOMe G.sub.3 Q225 H COOMe Gb CH.sub.2 - Q225 H COOMe Gc Q226 H COOMe G.sub.3 Q227 H COOMe Gc Q228 H COOMe Gc Q229 H COOMe Gb CH.sub.2 - Q229 H COOMe Gc Q230 HCOOMe Gc Q231 H COOMe Gc Q232 H COOMe G.sub.3 Q233 H COOMe Gc Q234 H COOMe Gc Q235 H COOMe Gc Q236 H COOMe G.sub.3 Q237 H COOMe Gc Q238 H COOMe Gc Q239 H COOMe G.sub.2 Q240 H COOMe Gc Q241 H COOMe Gc Q242 H COOMe Gc Q243 H COOMe G.sub.1 Q244 H COOMe Gc Q245 H COOMe Gc Q246 H COOMe Gb CH.sub.2 - Q246 H COOMe Gc Q247 H COOMe G.sub. 3 Q248 H COOMe Gc Q249 H COOMe Gc Q250 H COOMe Gc CH.sub.2 - Q250 H COOMe G.sub.3 Q251 H COOMe Gc Q252 H COOMe Gc Q253 H COOMe Gc Q254 H COOMeG.sub.1 Q255 H COOMe Gc Q256 H COOMe Gc Q257 H COOMe G.sub.3 Q258 H COOMe Gc Q259 H COOMe Gc CH.sub.2 - Q259 H COOMe Gc Q260 H COOMe Gc CH.sub.2 - Q260 H COOMe Gc Q261 H COOMe G.sub.1 Q262 H COOMe Gc Q263 H COOMe Gc Q264 H COOMe G.sub.2 Q201 H COOEt Ga CH.sub.2 - Q201 H COOEt Gb CHMe - Q201 H COOEt Gb Q202 H COOEt Gb CH.sub.2 - Q202 H COOEt Gb Q203 H COOEt Gb Q204 H COOEt Gb Q205 H COOEt Gb CH.sub.2 - Q205 H COOEt Gc Q206 H COOEt G.sub.3 Q207 H COOEt Gc Q208 H COOEtG.sub.3 Q209 H COOEt Gc CH.sub.2 - Q209 H COOEt Gc Q210 H COOEt Gc CH.sub.2 - 210 H COOEt G.sub.3 Q211 H COOEt Gc Q212 H COOEt Gc Q213 H COOEt Gc Q214 H COOEt G.sub.1 Q215 H COOEt Gc Q216 H COOEt Gc Q217 H COOEt G.sub.2 Q218 H COOEt Gc Q219 H COOEt Gc Q220 H COOEt G.sub.3 Q221 H COOEt Gc Q222 H COOEt Gb CH.sub.2 - Q222 H COOEt Gc Q223 H COOEt Gc Q224 H COOEt Gc Q225 H COOEt Gb CH.sub.2 - Q225 H COOEt Gc Q226 H COOEt G.sub.3 Q227 H COOEt Gc Q228 H COOEt Gc Q229 H COOEt Gb CH.sub.2 - Q229 H COOEt Gc Q230 H COOEt Gc Q231 H COOEt Gc Q232 H COOEt G.sub.3 Q233 H COOEt Gc Q234 H COOEt Gc CH.sub.2 - Q234 H COOEt Gc Q235 H COOEt Gc Q236 H COOEt G.sub.3 Q237 H COOEt Gc Q238 H COOEt Gc Q239 H COOEt Gc Q240 H COOEtG.sub.1 Q241 H COOEt Gc Q242 H COOEt Gc Q243 H COOEt Gc Q244 H COOEt G.sub.2 Q245 H COOEt Gc Q246 H COOEt Gb CH.sub.2 - Q246 H COOEt Gc Q247 H COOEt Gc Q248 H COOEt Gc Q249 H COOEt G.sub.3 Q250 H COOEt Gc CH.sub.2 - Q250 H COOEt Gc Q251 HCOOEt Gc Q252 H COOEt G.sub.3 Q253 H COOEt Gc Q254 H COOEt Gc Q255 H COOEt Gc Q256 H COOEt Gc Q257 H COOEt Gc Q258 H COOEt G.sub.1 Q259 H COOEt Gc CH.sub.2 - Q259 H COOEt Gc Q260 H COOEt Gc CH.sub.2 - Q260 H COOEt Gc Q261 H COOEt G.sub.3 Q262 H COOEt Gc Q263 H COOEt Gc Q264 H COOEt G.sub.3 Q201 H COOH Gc Q202 H COOH Gc Q222 H COOH Gc Q225 H COOH G.sub.3 Q229 H COOH Gc Q246 H COOH G.sub.3 Q201 H COOPri Gc Q202 H COOPri G.sub.3 Q205 H COOPri Gc Q209 H COOPri Gc Q222 H COOPriGc Q225 H COOPri Gc Q229 H COOPri G.sub.3 Q246 H COOPri Gc Q201 H COOCH.sub.2 CH.sub.2 Cl Gc Q202 H COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q205 H COOCH.sub.2 CH.sub.2 Cl Gc Q209 H COOCH.sub.2 CH.sub.2 Cl Gc Q222 H COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q225 H COOCH.sub.2 CH.sub.2 Cl Gc Q229 H COOCH.sub.2 CH.sub.2 Cl Gc Q246 H COOCH.sub.2 CH.sub.2 Cl G.sub.1 Q201 H COOCH.sub.2 CHCH.sub.2 Gc Q202 H COOCH.sub.2 CHCH.sub.2 Gc Q205 H COOCH.sub.2 CHCH.sub.2 G.sub.3 Q209 H COOCH.sub.2 CHCH.sub.2 Gc Q222 H COOCH.sub.2 CHCH.sub.2 Gc Q225 H COOCH.sub.2 CHCH.sub.2 Gc Q229 H COOCH.sub.2 CHCH.sub.2 G.sub.3 Q246 H COOCH.sub.2 CHCH.sub.2 Gc Q201 H COOCH.sub.2 CCH Gc Q202 H COOCH.sub.2 CCH G.sub.3 Q205 H COOCH.sub.2 CCH Gc Q209 HCOOCH.sub.2 CCH Gc Q222 H COOCH.sub.2 CCH Gc Q225 H COOCH.sub.2 CCH G.sub.3 Q229 H COOCH.sub.2 CCH Gc Q246 H COOCH.sub.2 CCH G.sub.3 Q201 H CONHMe Gc Q202 H CONHMe G.sub.3 Q205 H CONHMe Gc Q209 H CONHMe Gc Q222 H CONHMe G.sub.3 Q225 HCONHMe Gc Q229 H CONHMe Gc Q246 H CONHMe G.sub.3 Q201 H CONMe.sub.2 Gc Q202 H CONMe.sub.2 G.sub.3 Q205 H CONMe.sub.2 Gc Q209 H CONMe.sub.2 Gc Q222 H CONMe.sub.2 Gc Q225 H CONMe.sub.2 G.sub.3 Q229 H CONMe.sub.2 Gc Q246 H CONMe.sub.2 G.sub.2 Q201 H COMe Gc CH.sub.2 - Q201 H COMe G.sub.3 Q202 H COMe G.sub.3 Q205 H COMe Gc Q207 H COMe G.sub.3 Q222 H COMe Gc Q225 H COMe Gc Q229 H COMe Gc Q230 H COMe G.sub.2 Q231 H COMe G.sub.3 Q237 H COMe Gc Q246 H COMe Gc Q247 H COMe G.sub.3 Q250 H COMe Gc Q259 H COMe Gc Q260 H COMe Gc Q263 H COMe G.sub.3 Q201 H COEt Gc Q202 H COEt G.sub.3 Q205 H COEt Gc Q209 H COEt Gc Q222 H COEt Gc Q225 H COEt G.sub.3 Q229 H COEt Gc Q246 H COEt G.sub.3 Q201 H COPri Gc Q202 H COPri G.sub.3 Q205 H COPri Gc Q209 H COPri Gc Q222 H COPri Gc Q225 H COPri G.sub.3 Q229 H COPri Gc Q246 H COPri Gc Q201 H COPh Gc Q202 H COPh G.sub.3 Q205 H COPh Gc Q209 H COPh Gc Q222 H COPhG.sub.3 Q225 H COPh Gc Q229 H COPh Gc Q246 H COPh G.sub.3 Q201 H CN Gc CH.sub.2 - Q201 H CN G.sub.3 Q202 H CN Gc Q205 H CN Gc Q209 H CN Gc Q222 H CN Gc Q225 H CN Gc Q229 H CN Gc Q246 H CN G.sub.3 Q201 H H Gc Q202 H H G.sub.3 Q205 H H Gc Q207 H H Gc Q222 H H Gc Q225 H H G.sub.3 Q229 H H Gc Q230 H H Gc Q231 H H G.sub.3 Q237 H H Gc Q246 H H Gc Q247 H H G.sub.3 Q250 H H Gc Q259 H H G.sub.3 Q260 H H Gc Q263 H H G.sub.3 Q201 H Me Gc Q202 H Me G.sub.3 Q205 H Me Gc Q207 H MeG.sub.3 Q222 H Me Gc Q225 H Me Gc Q229 H Me Gc Q230 H Me G.sub.3 Q231 H Me Gc Q237 H Me Gc Q246 H Me Gc Q247 H Me G.sub.3 Q250 H Me Gc Q259 H Me Gc Q260 H Me Gc Q263 H Me G.sub.3 Q201 H Et Gc Q202 H Et G.sub.1 Q205 H Et Gc Q209 H Et Gc Q222 H Et G.sub.3 Q225 H Et Gc Q229 H Et Gc Q246 H Et G.sub.2 Q201 H Pri Gc Q205 H Pri Gc Q209 H Pri Gc Q222 H Pri G.sub.3 Q229 H Pri Gc Q201 H CHCH.sub.2 Gc Q205 H CHCH.sub.2 G.sub.3 Q209 H CHCH.sub.2 Gc Q229 H CHCH.sub.2 G.sub.3 Q201 HCHCHMe Gc Q205 H CHCHMe Gc Q201 H CH.sub.2 CHCH.sub.2 Gc Q205 H CH.sub.2 CHCH.sub.2 G.sub.3 Q209 H CH.sub.2 CHCH.sub.2 Gc Q229 H CH.sub.2 CHCH.sub.2 Gc Q201 H CH.sub.2 Cl Gc Q205 H CH.sub.2 Cl G.sub.3 Q209 H CH.sub.2 Cl Gc Q229 H CH.sub.2 ClGc Q201 H CH.sub.2 CH.sub.2 Cl Gc Q205 H CH.sub.2 CH.sub.2 Cl G.sub.3 Q209 H CH.sub.2 CH.sub.2 Cl Gc Q229 H CH.sub.2 CH.sub.2 Cl G.sub.2 Q201 H CF.sub.3 Gc Q205 H CF.sub.3 G.sub.3 Q209 H CF.sub.3 Gc Q222 H CF.sub.3 Gc Q225 H CF.sub.3 G.sub.3 Q229 H CF.sub.3 G.sub.1 Q201 H CFCFCl Gc Q205 H CFCFCl Gc Q229 H CFCFCl G.sub.3 Q201 H CH.sub.2 Ph Gc Q205 H CH.sub.2 Ph Gc Q209 H CH.sub.2 Ph G.sub.3 Q201 H Ph Gc Q202 H Ph G.sub.1 Q205 H Ph Gc Q209 H Ph Gc Q222 H Ph G.sub.3 Q225 H Ph Gc Q229 H Ph Gc Q246 H Ph G.sub.2 Q201 H Ph2-Cl Gc Q205 H Ph2-Cl G.sub.1 Q209 H Ph2-Cl Gc Q201 H Ph2-Me Gc Q205 H Ph2-Me G.sub.3 Q209 H Ph2-Me Gc Q225 H Ph2-Me Gc Q229 H Ph2-Me G.sub.3 Q201 H Cl Gc Q205 H Cl Gc Q207 H Cl G.sub.3 Q222 H Cl Gc Q225 H Cl Gc Q229 H Cl G.sub.1 Q231 H Cl Gc Q246 H Cl Gc Q250 H Cl G.sub.3 Q259 H Cl Gc Q260 H Cl Gc Q201 H Br Gc Q205 H Br G.sub.3 Q207 H Br Gc Q229 H Br Gc Q231 H Br G.sub.3 Q250 H Br Gc Q259 H Br Gc Q260 H Br G.sub.3 Q201 H F Gc Q205 HF G.sub.3 Q209 H F Gc Q229 H F Gc Q246 H F G.sub.3 Q201 H I Gc Q205 H I Gc Q209 H I Gc Q222 H I Gc Q201 H NO.sub.2 Gc CH.sub.2 - Q201 H NO.sub.2 G.sub.3 Q202 H NO.sub.2 G.sub.3 Q205 H NO.sub.2 Gc Q207 H NO.sub.2 Gc Q222 H NO.sub.2 G.sub.3 Q225 H NO.sub.2 Gc Q229 H NO.sub.2 Gc Q230 H NO.sub.2 G.sub.1 Q231 H NO.sub.2 Gc Q237 H NO.sub.2 Gc Q246 H NO.sub.2 Gc Q247 H NO.sub.2 G.sub.2 Q250 H NO.sub.2 Gc Q259 H NO.sub.2 Gc Q260 H NO.sub.2 G.sub.3 Q263 H NO.sub.2 Gc Q201 H NH.sub. 2 Gc Q202 H NH.sub.2 G.sub.3 Q205 H NH.sub.2 Gc Q209 H NH.sub.2 Gc Q222 H NH.sub.2 G.sub.3 Q225 H NH.sub.2 Gc Q229 H NH.sub.2 Gc Q246 H NH.sub.2 G.sub.3 Q201 H NHMe Gc Q205 H NHMe Gc Q209 H NHMe Gc Q225 H NHMe Gc Q229 H NHMe G.sub.3 Q201 HNMe.sub.2 Gc Q205 H NMe.sub.2 Gc Q209 H NMe.sub.2 Gc Q222 H NMe.sub.2 G.sub.1 Q225 H NMe.sub.2 Gc Q229 H NMe.sub.2 Gc Q246 H NMe.sub.2 G.sub.3 Q201 H NMeEt Gc Q205 H NMeEt Gc Q209 H NMeEt G.sub.3 Q222 H NMeEt Gc Q225 H NMeEt Gc Q229 H NMeEtG.sub.2 Q201 H NHCOMe Gc Q202 H NHCOMe G.sub.3 Q205 H NHCOMe Gc Q209 H NHCOMe Gc Q222 H NHCOMe G.sub.3 Q225 H NHCOMe Gc Q229 H NHCOMe Gc Q246 H NHCOMe G.sub.3 Q201 H NHCOEt Gc Q205 H NHCOEt Gc Q209 H NHCOEt Gc Q222 H NHCOEt G.sub.1 Q225 HNHCOEt Gc Q229 H NHCOEt G.sub.3 Q201 H NHSO.sub.2 Me Gc Q205 H NHSO.sub.2 Me Gc Q209 H NHSO.sub. 2 Me Gc Q225 H NHSO.sub.2 Me G.sub.3 Q229 H NHSO.sub.2 Me G.sub.3 Q201 H OMe Gc Q205 H OMe Gc Q209 H OMe G.sub.3 Q222 H OMe Gc Q225 H OMe Gc Q229H OMe G.sub.2 Q246 H OMe G.sub.1 Q201 H OEt Gc Q205 H OEt Gc Q209 H OEt Gc Q222 H OEt G.sub.3 Q229 H OEt Gc Q201 H CH.sub.2 OMe Gc Q205 H CH.sub.2 OMe Gc Q209 H CH.sub.2 OMe G.sub.3 Q222 H CH.sub.2 OMe Gc Q201 H SMe Gc Q205 H SMe Gc Q209 HSMe Gc Q222 H SMe G.sub.1 Q225 H SMe Gc Q229 H SMe G.sub.3 Q201 H SO.sub.2 Me Gc CH.sub.2 - Q201 H SO.sub.2 Me G.sub.3 Q202 H SO.sub.2 Me Gc Q205 H SO.sub.2 Me Gc Q209 H SO.sub.2 Me Gc Q222 H SO.sub.2 Me G.sub.3 Q225 H SO.sub.2 Me Gc Q229 H SO.sub.2 Me Gc Q246H SO.sub.2 Me G.sub.3 Q201 H SO.sub.2 Ph Gc Q202 H SO.sub.2 Ph G.sub.1 Q205 H SO.sub.2 Ph Gc Q209 H SO.sub.2 Ph Gc Q222 H SO.sub.2 Ph Gc Q225 H SO.sub.2 Ph G.sub.3 Q229 H SO.sub.2 Ph Gc Q246 H SO.sub.2 Ph G.sub.1 Q201 H SO.sub.2 OMe Gc Q205 HSO.sub.2 OMe Gc Q209 H SO.sub.2 OMe Gc Q222 H SO.sub.2 OMe Gc Q229 H SO.sub.2 OMe G.sub.3 Q201 H SO.sub.2 NH.sub.2 Gc Q205 H SO.sub.2 NH.sub.2 Gc Q209 H SO.sub.2 NH.sub.2 G.sub.3 Q225 H SO.sub.2 NH.sub.2 Gc Q229 H SO.sub.2 NH.sub.2 Gc Q246H SO.sub.2 NH.sub.2 G.sub.1 Q201 H SO.sub.2 NHMe Gc Q205 H SO.sub.2 NHMe Gc Q209 H SO.sub.2 NHMe G.sub.3 Q222 H SO.sub.2 NHMe Gc Q225 H SO.sub.2 NHMe Gc Q229 H SO.sub.2 NHMe Gc Q246 H SO.sub.2 NHMe G.sub.2 Q201 H SO.sub.2 NMe.sub.2 Gc Q202 HSO.sub.2 NMe.sub.2 G.sub.3 Q205 H SO.sub.2 NMe.sub.2 Gc Q209 H SO.sub.2 NMe.sub.2 Gc Q222 H SO.sub.2 NMe.sub.2 G.sub.2 Q225 H SO.sub.2 NMe.sub.2 Gc Q229 H SO.sub.2 NMe.sub. 2 Gc Q246 H SO.sub.2 NMe.sub.2 G.sub.3 Q201 Me COOMe Gc CH.sub.2 -Q201 Me COOMe G.sub.3 Q201 Me COOMe G.sub.1 Q205 Me COOMe Gc Q207 Me COOMe G.sub.3 Q209 Me COOMe Gc Q222 Me COOMe Gc Q225 Me COOMe G.sub.2 Q229 Me COOMe Gc Q230 Me COOMe Gc Q231 Me COOMe G.sub.3 Q237 Me COOMe Gc Q246 Me COOMe Gc Q247 MeCOOMe G.sub.3 Q250 Me COOMe Gc Q259 Me COOMe G.sub.1 Q260 Me COOMe Gc Q263 Me COOMe G.sub.3 Q201 Me COOEt Gc CH.sub.2 - Q201 Me COOEt G.sub.2 Q222 Me COOEt Gc Q205 Me COOEt Gc Q207 Me COOEt G.sub.3 Q209 Me COOEt Gc Q222 Me COOEt Gc Q225 MeCOOEt G.sub.3 Q229 Me COOEt Gc Q230 Me COOEt Gc Q231 Me COOEt Gc Q237 Me COOEt G.sub.1 Q246 Me COOEt Gc Q247 Me COOEt Gc Q250 Me COOEt Gc Q259 Me COOEt G.sub.3 Q260 Me COOEt Gc Q263 Me COOEt G.sub.3 Q201 Me COOH G.sub.1 Q205 Me COOH Gc Q201Me COOPri Gc Q202 Me COOPri G.sub.3 Q205 Me COOPri Gc Q209 Me COOPri Gc Q222 Me COOPri G.sub.3 Q225 Me COOPri Gc Q229 Me COOPri Gc Q246 Me COOPri G.sub.1 Q201 Me COOCH.sub.2 CH.sub.2 Cl Gc Q205 Me COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q222 MeCOOCH.sub.2 CH.sub.2 Cl Gc Q229 Me COOCH.sub.2 CH.sub.2 Cl G.sub.1 Q201 Me COOCH.sub.2 CHCH.sub.2 Gc Q205 Me COOCH.sub.2 CHCH.sub.2 G.sub.3 Q222 Me COOCH.sub.2 CHCH.sub.2 Gc Q229 Me COOCH.sub.2 CHCH.sub.2 G.sub.1 Q201 Me COOCH.sub.2 CCH Gc Q205 Me COOCH.sub.2 CCH G.sub.2 Q222 Me COOCH.sub.2 CCH Gc Q229 Me COOCH.sub.2 CCH Gc Q201 Me CONHMe Gc Q205 Me CONHMe G.sub.3 Q222 Me CONHMe Gc Q229 Me CONHMe Gc Q201 Me CONMe.sub.2 Gc Q205 Me CONMe.sub.2 G.sub.3 Q222 Me CONMe.sub.2 Gc Q229Me CONMe.sub.2 Gc Q201 Me COMe Gc Q202 Me COMe G.sub.3 Q205 Me COMe Gc Q207 Me COMe Gc Q222 Me COMe G.sub.3 Q225 Me COMe Gc Q229 Me COMe Gc Q230 Me COMe G.sub.3 Q231 Me COMe Gc Q237 Me COMe Gc Q246 Me COMe Gc Q247 Me COMe G.sub.2 Q250 MeCOMe Gc Q259 Me COMe Gc Q260 Me COMe G.sub.1 Q263 Me COMe Gc Q201 Me COEt Gc Q205 Me COEt G.sub.3 Q222 Me COEt Gc Q229 Me COEt Gc Q201 Me COPri Gc Q205 Me COPri G.sub.3 Q222 Me COPri Gc Q229 Me COPri G.sub.1 Q201 Me COPh Gc Q205 Me COPh Gc Q222 Me COPh G.sub.3 Q229 Me COPh Gc Q201 Me CN Gc Q202 Me CN G.sub.3 Q205 Me CN Gc Q209 Me CN Gc Q222 Me CN G.sub.3 Q225 Me CN Gc Q229 Me CN Gc Q246 Me CN G.sub.1 Q201 Me H Gc Q205 Me H Gc Q222 Me H G.sub.3 Q229 Me H Gc Q201 Me Me Gc Q202Me Me G.sub.3 Q205 Me Me Gc Q209 Me Me Gc Q222 Me Me Gc Q225 Me Me Gc Q229 Me Me G.sub.3 Q246 Me Me Gc Q201 Me Et Gc Q205 Me Et Gc Q222 Me Et G.sub.3 Q229 Me Et Gc Q201 Me Pri Gc Q205 Me Pri G.sub.2 Q201 Me CHCH.sub.2 Gc Q205 Me CHCH.sub.2G.sub.3 Q201 Me CHCHMe G.sub.3 Q205 Me CHCHMe Gc Q201 Me CH.sub.2 CHCH.sub.2 Gc Q205 Me CH.sub.2 CHCH.sub.2 G.sub.3 Q201 Me CH.sub.2 Cl Gc Q205 Me CH.sub.2 Cl G.sub.2 Q222 Me CH.sub.2 Cl Gc Q229 Me CH.sub.2 Cl G.sub.3 Q201 Me CH.sub.2 CH.sub.2Cl Gc Q205 Me CH.sub.2 CH.sub.2 Cl Gc Q222 Me CH.sub.2 CH.sub.2 Cl G.sub.3 Q229 Me CH.sub.2 CH.sub.2 Cl Gc Q201 Me CF.sub.3 Gc Q205 Me CF.sub.3 G.sub.3 Q222 Me CF.sub.3 G.sub.3 Q229 Me CF.sub.3 Gc Q201 Me CFCFCl Gc Q205 Me CFCFCl G.sub.3 Q201 Me CH.sub.2 Ph Gc Q205 Me CH.sub.2 Ph G.sub.3 Q201 Me Ph Gc Q202 Me Ph Gc Q205 Me Ph Gc Q209 Me Ph Gc Q222 Me Ph G.sub.3 Q225 Me Ph G.sub.3 Q229 Me Ph Gc Q246 Me Ph G.sub.3 Q201 Me Ph2-Cl Gc Q205 Me Ph2-Cl G.sub.3 Q201 Me Ph2-Me Gc Q205Me Ph2-Me Gc Q229 Me Ph2-Me G.sub.3 Q201 Me Cl Gc Q202 Me Cl G.sub.3 Q205 Me Cl Gc Q209 Me Cl Gc Q222 Me Cl G.sub.3 Q225 Me Cl Gc Q229 Me Cl Gc Q246 Me Cl G.sub.3 Q201 Me Br Gc Q205 Me Br G.sub.3 Q222 Me Br Gc Q229 Me Br G.sub.1 Q201 Me FG.sub.1 Q205 Me F G.sub.1 Q201 Me I G.sub.1 Q205 Me I G.sub.1 Q201 Me NO.sub.2 Gc Q202 Me NO.sub.2 G.sub.3 Q205 Me NO.sub.2 Gc Q209 Me NO.sub.2 Gc Q222 Me NO.sub.2 Gc Q225 Me NO.sub.2 G.sub.3 Q229 Me NO.sub.2 Gc Q246 Me NO.sub.2 Gc Q201 Me NH.sub.2 Gc Q205 Me NH.sub.2 G.sub.3 Q222 Me NH.sub.2 Gc Q229 Me NH.sub.2 G.sub.3 Q201 Me NHMe Gc Q205 Me NHMe Gc Q229 Me NHMe G.sub.3 Q201 Me NMe.sub.2 Gc Q205 Me NMe.sub.2 Gc Q229 Me NMe.sub.2 G.sub.3 Q201 Me NMeEt Gc Q205 Me NMeEt Gc Q201 Me NHCOMe Gc Q205 Me NHCOMe Gc Q222 Me NHCOMe G.sub.3 Q229 Me NHCOMe Gc Q201 Me NHCOEt Gc Q205 Me NHCOEt G.sub.3 Q201 Me NHSO.sub.2 Me Gc Q205 Me NHSO.sub.2 Me Gc Q229 Me NHSO.sub.2 Me G.sub.2 Q201 Me OMe Gc Q205 Me OMe G.sub.3 Q222 Me OMe Gc Q229 Me OMe G.sub.1 Q201 Me OEt Gc Q205 Me OEt G.sub.3 Q201 Me CH.sub.2 OMe Gc Q205 Me CH.sub.2 OMe Gc Q229 Me CH.sub.2 OMe G.sub.3 Q201 Me SMe Gc Q205 Me SMe G.sub.3 Q201 Me SO.sub.2 Me Gc Q205 Me SO.sub.2 Me Gc Q222 Me SO.sub.2 Me G.sub.1 Q229 Me SO.sub.2 Me G.sub.3 Q201 Me SO.sub.2 Ph Gc Q205 MeSO.sub.2 Ph Gc Q222 Me SO.sub.2 Ph G.sub.3 Q229 Me SO.sub.2 Ph Gc Q201 Me SO.sub.2 OMe Gc Q205 Me SO.sub.2 OMe G.sub.3 Q229 Me SO.sub.2 OMe Gc Q201 Me SO.sub.2 NH.sub.2 Gc Q205 Me SO.sub.2 NH.sub.2 Gc Q229 Me SO.sub.2 NH.sub.2 G.sub.3 Q201 MeSO.sub.2 NHMe Gc Q205 Me SO.sub.2 NHMe Gc Q222 Me SO.sub.2 NHMe G.sub.1 Q229 Me SO.sub.2 NHMe Gc Q201 Me SO.sub.2 NMe.sub.2 Gc Q205 Me SO.sub.2 NMe.sub.2 G.sub.3 Q222 Me SO.sub.2 NMe.sub.2 Gc Q229 Me SO.sub.2 NMe.sub.2 G.sub.1 Q201 Et COOMeGc Q205 Et COOMe Gc Q229 Et COOMe G.sub.3 Q246 Et COOMe G.sub.3 Q201 Et COOEt Gc Q202 Et COOEt G.sub.2 Q209 Et COOEt Gc Q222 Et COOEt G.sub.3 Q225 Et COOEt Gc Q201 Et COOPri G.sub.3 Q205 Et COOPri Gc Q201 Et COOCH.sub.2 CHCl Gc Q205 EtCOOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 Et COOCH.sub.2 CCH Gc Q201 Et CONHMe Gc Q201 Et CONMe.sub.2 Gc Q201 Et COMe Gc Q205 Et COMe G.sub.3 Q229 Et COMe Gc Q201 Et COEt Gc Q201 Et COPh Gc Q201 Et CN Gc Q205 Et CN G.sub.3 Q229 Et CN Gc Q201 Et HGc Q205 Et H G.sub.3 Q201 Et Me Gc Q205 Et Me G.sub.3 Q201 Et Et Gc Q205 Et Pri Gc Q201 Et CHCHMe Gc Q201 Et CH.sub.2 CH.sub.2 Cl Gc Q201 Et CH.sub.2 Ph G.sub.3 Q201 Et Ph Gc Q205 Et Ph Gc Q209 Et Ph Gc Q229 Et Ph G.sub.3 Q201 Et Ph2-Cl Gc Q205 Et Ph2-Me Gc Q201 Et Cl Gc Q205 Et Cl G.sub.2 Q201 Et BrGc Q205 Et Br G.sub.1 Q201 Et F Gc Q201 Et NO.sub.2 Gc Q205 Et NO.sub.2 G.sub.3 Q209 Et NO.sub.2 Gc Q201 Et NH.sub.2 Gc Q201 Et NHMe Gc Q201 Et NMe.sub.2 Gc Q205 Et NMe.sub.2 G.sub.3 Q201 Et NHCOMe Gc Q205 Et NHCOMe Gc Q201 Et NHCOEt Gc Q201Et NHSO.sub.2 Me Gc Q201 Et OMe Gc Q205 Et OEt G.sub.3 Q201 Et CH.sub.2 OMe Gc Q201 Et SMe Gc Q201 Et SO.sub.2 Me Gc Q205 Et SO.sub.2 Me G.sub.3 Q201 Et SO.sub.2 Ph Gc Q205 Et SO.sub.2 Ph G.sub.3 Q201 Et SO.sub.2 OMe Gc Q201 Et SO.sub.2NH.sub.2 Gc Q205 Et SO.sub.2 NHMe G.sub.3 Q201 Et SO.sub. 2 NMe.sub.2 Gc Q205 Et SO.sub.2 NMe.sub.2 G.sub.3 Q201 Cl COOMe Gc Q209 Cl COOMe G.sub.3 Q229 Cl COOMe Gc Q246 Cl COOMe G.sub.3 Q201 Cl COOEt Gc Q205 Cl COOEt Gc Q222 Cl COOEt G.sub.1 Q225 Cl COOEt Gc Q246 Cl COOEt G.sub.3 Q201 Cl COOPri Gc Q205 Cl COOPri G.sub.3 Q205 Cl COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Cl COOCH.sub.2 CHCH.sub.2 Gc Q201 Cl COOCH.sub.2 CCH G.sub.3 Q201 Cl CONHMe Gc Q201 Cl CONMe.sub.2 G.sub.3 Q201 ClCOMe Gc Q205 Cl COMe Gc Q201 Cl COEt G.sub.3 Q201 Cl COPri Gc Q201 Cl COPh G.sub.3 Q201 Cl CN Gc Q205 Cl CN Gc Q201 Cl H G.sub.3 Q201 Cl Me Gc Q205 Cl Me G.sub.3 Q205 Cl Et Gc Q201 Cl Pri G.sub.3 Q201 Cl CHCHMe Gc Q201 Cl CH.sub.2 CHCH.sub.2 G.sub.1 Q205 Cl CH.sub.2 CH.sub.2 Cl Gc Q201 Cl Ph Gc Q205 Cl Ph Gc Q209 Cl Ph G.sub.3 Q201 Cl Ph2-Cl Gc Q205 Cl Ph2-Me G.sub.3 Q201 Cl Cl Gc Q205 Cl Cl G.sub.3 Q201 Cl Br Gc Q201 Cl NO.sub.2 Gc Q205 Cl NO.sub.2 G.sub.3 Q209 Cl NO.sub.2 Gc Q201 Cl NH.sub.2 Gc Q201 Cl NHMe G.sub.1 Q201 Cl NMe.sub.2 G.sub.3 Q201 Cl NHCOMe Gc Q205 Cl NHCOEt Gc Q201 Cl NHSO.sub.2 Me G.sub.3 Q201 Cl OMe Gc Q201 Cl CH.sub.2 OMe G.sub.3 Q201 Cl SO.sub.2 Me Gc Q201 Cl SO.sub.2 Ph Gc Q201 Cl SO.sub.2NH.sub.2 G.sub.3 Q201 Cl SO.sub.2 NMe.sub.2 Gc Q205 Cl SO.sub.2 NMe.sub.2 Gc Q201 Br COOMe Gc Q205 Br COOMe G.sub.3 Q209 Br COOMe G.sub.3 Q201 Br COOEt Gc Q209 Br COOEt Gc Q229 Br COOEt G.sub.3 Q201 Br COOPri G.sub.3 Q201 Br COOCH.sub.2 CHCl Gc Q201 Br COOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 Br CONHMe Gc Q201 Br CONMe.sub.2 G.sub.3 Q201 Br COMe Gc Q205 Br COMe G.sub.3 Q201 Br COEt Gc Q201 Br COPh G.sub.3 Q201 Br CN Gc Q205 Br CN Gc Q201 Br H G.sub.3 Q201 Br Me G.sub.2 Q201 Br EtG.sub.1 Q201 Br CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Br Ph Gc Q205 Br Ph Gc Q209 Br Ph G.sub.3 Q201 Br Ph2-Cl G.sub.3 Q201 Br Cl Gc Q201 Br Br Gc Q205 Br Br G.sub.3 Q201 Br NO.sub.2 Gc Q209 Br NO.sub.2 Gc Q201 Br NH.sub.2 Gc Q201 Br NMe.sub.2G.sub.3 Q201 Br NHCOMe Gc Q201 Br OMe G.sub.3 Q201 Br CH.sub.2 OMe Gc Q201 Br SMe Gc Q201 Br SO.sub.2 Me Gc Q201 Br SO.sub.2 NH.sub.2 G.sub.3 Q201 Br SO.sub.2 NHMe Gc Q201 Br SO.sub.2 NMe.sub.2 G.sub.3 Q201 SMe COOMe Gc Q205 SMe COOMe Gc Q209 SMe COOMe G.sub.3 Q201 SMe COOEt Gc Q205 SMe COOEt Gc Q209 SMe COOEt Gc Q229 SMe COOEt G.sub.3 Q246 SMe COOEt Gc Q201 SMe COOPri Gc Q205 SMe COOPri G.sub.3 Q201 SMe COOCH.sub.2 CH.sub.2 Cl Gc Q201 SMe COOCH.sub.2 CHCH.sub.2 Gc Q201 SMeCONHMe Gc Q201 SMe CONMe.sub.2 G.sub.1 Q201 SMe COMe Gc Q205 SMe COMe Gc Q201 SMe COEt G.sub.3 Q201 SMe COPri Gc Q201 SMe COPh G.sub.3 Q201 SMe CN Gc Q205 SMe CN Gc Q229 SMe CN G.sub.3 Q201 SMe H Gc Q201 SMe Me Gc Q205 SMe Me G.sub.3 Q201SMe Et Gc Q205 SMe Et Gc Q201 SMe CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 SMe Ph Gc Q205 SMe Ph Gc Q209 SMe Ph G.sub.3 Q201 SMe Ph2-Cl Gc Q201 SMe Cl Gc Q205 SMe Cl G.sub.3 Q201 SMe Br Gc Q201 SMe NO.sub.2 Gc Q205 SMe NO.sub.2 Gc Q209 SMe NO.sub.2G.sub.3 Q201 SMe NH.sub.2 Gc Q205 SMe NH.sub.2 Gc Q201 SMe NHMe G.sub.3 Q201 SMe NMe.sub.2 Gc Q205 SMe NMe.sub.2 Gc Q201 SMe NHCOMe Gc Q205 SMe NHCOMe G.sub.3 Q201 SMe NHSO.sub.2 Me Gc Q201 SMe OMe Gc Q201 SMe CH.sub.2 OMe Gc Q201 SMe SMe Gc Q201 SMe SO.sub.2 Me Gc Q205 SMe SO.sub.2 Me G.sub.3 Q201 SMe SO.sub.2 Ph Gc Q201 SMe SO.sub.2 NH.sub.2 Gc Q201 SMe SO.sub.2 NHMe G.sub.3 Q201 SMe SO.sub.2 NMe.sub.2 Gc Q201 SO.sub.2 Me COOMe Gc Q205 SO.sub.2 Me COOMe Gc Q209 SO.sub.2 Me COOMe G.sub.3 Q229 SO.sub.2 Me COOMe G.sub.3 Q246 SO.sub.2 Me COOMe G.sub.1 Q201 SO.sub.2 Me COOEt Gc Q205 SO.sub.2 Me COOEt Gc Q209 SO.sub.2 Me COOEt G.sub.3 Q222 SO.sub.2 Me COOEt Gc Q225 SO.sub.2 Me COOEt Gc Q201 SO.sub.2 Me COOPriG.sub.3 Q205 SO.sub.2 Me COOPri Gc Q201 SO.sub.2 Me COOCH.sub.2 CH.sub.2 Cl Gc Q201 SO.sub.2 Me COOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 SO.sub.2 Me COOCH.sub.2 CCH Gc Q201 SO.sub.2 Me CONHMe Gc Q201 SO.sub.2 Me CONMe.sub.2 G.sub.2 Q201SO.sub.2 Me COMe Gc Q205 SO.sub.2 Me COMe Gc Q229 SO.sub.2 Me COMe G.sub.3 Q201 SO.sub.2 Me COEt Gc Q205 SO.sub.2 Me COEt Gc Q201 SO.sub.2 Me COPri G.sub.3 Q201 SO.sub.2 Me COPh Gc Q201 SO.sub.2 Me CN Gc Q205 SO.sub.2 Me CN Gc Q222 SO.sub.2 Me CN Gc Q229 SO.sub.2Me CN Gc Q201 SO.sub.2 Me H G.sub.2 Q201 SO.sub.2 Me Me Gc Q205 SO.sub.2 Me Me Gc Q201 SO.sub.2 Me Et G.sub.3 Q201 SO.sub.2 Me Pri Gc Q201 SO.sub.2 Me CHCH.sub.2 Gc Q201 SO.sub.2 Me CHCHMe G.sub.1 Q201 SO.sub.2 Me CH.sub.2 CH.sub.2 Cl Gc Q205 SO.sub.2 Me CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 SO.sub.2 Me CH.sub.2 Ph G.sub.3 Q201 SO.sub.2 Me Ph Gc Q205 SO.sub.2 Me Ph Gc Q209 SO.sub.2 Me Ph Gc Q229 SO.sub.2 Me Ph G.sub.3 Q246 SO.sub.2 Me Ph G.sub.3 Q201 SO.sub.2 Me Ph2-Cl Gc Q205 SO.sub.2 Me Ph2-Me Gc Q201 SO.sub.2 Me Cl Gc Q205 SO.sub.2 Me Cl Gc Q229 SO.sub.2 Me Cl G.sub.3 Q201 SO.sub.2 Me Br G.sub.3 Q205 SO.sub.2 Me Br Gc Q201 SO.sub.2 Me NO.sub.2 Gc Q205 SO.sub.2 Me NO.sub.2 Gc Q209 SO.sub.2 Me NO.sub.2Gc Q229 SO.sub.2 Me NO.sub.2 G.sub.3 Q201 SO.sub.2 Me NH.sub.2 Gc Q205 SO.sub.2 Me NH.sub.2 G.sub.3 Q201 SO.sub.2 Me NHMe Gc Q201 SO.sub.2 Me NMe.sub.2 Gc Q205 SO.sub.2 Me NMe.sub.2 G.sub.1 Q201 SO.sub.2 Me NHCOMe Gc Q205 SO.sub.2 Me NHCOMe Gc Q201 SO.sub.2 Me NHCOEt G.sub.3 Q201 SO.sub.2 Me NHSO.sub.2 Me Gc Q201 SO.sub.2 Me OMe G.sub.1 Q201 SO.sub.2 Me CH.sub.2 OMe Gc Q205 SO.sub.2 Me CH.sub.2 OMe Gc Q201 SO.sub.2 Me SO.sub.2 Me Gc Q205 SO.sub.2 Me SO.sub.2 Me Gc Q201SO.sub.2 Me SO.sub.2 Ph G.sub.3 Q201 SO.sub.2 Me SO.sub.2 OMe Gc Q201 SO.sub.2 Me SO.sub.2 NH.sub.2 Gc Q201 SO.sub.2 Me SO.sub.2 NHMe G.sub.3 Q201 SO.sub.2 Me SO.sub.2 NMe.sub.2 Gc Q201 Ph COOMe Gc Q205 Ph COOMe G.sub.3 Q209 Ph COOMe Gc Q201 Ph COOEt Gc Q205 Ph COOEt Gc Q209 Ph COOEt G.sub.3 Q229 Ph COOEt Gc Q201 Ph COOPri G.sub.3 Q201 Ph COOCH.sub.2 CH.sub.2 Cl Gc Q201 Ph COOCH.sub.2 CHCH.sub.2 Gc Q201 Ph COOCH.sub.2 CCH G.sub.3 Q201 Ph CONMe.sub.2 Gc Q201 Ph COMe Gc Q205Ph COMe Gc Q201 Ph COEt G.sub.3 Q201 Ph CN Gc Q205 Ph CN Gc Q201 Ph H G.sub.3 Q201 Ph Me Gc Q201 Ph Et Gc Q201 Ph CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Ph Ph Gc Q205 Ph Ph Gc Q209 Ph Ph G.sub.3 Q201 Ph Cl Gc Q201 Ph Br G.sub.3 Q201 Ph NO.sub.2Gc Q201 Ph NH.sub.2 Gc Q201 Ph NHMe G.sub.3 Q201 Ph NMe.sub.2 Gc Q201 Ph NHCOMe Gc Q201 Ph NHSO.sub.2 Me G.sub.1 Q201 Ph CH.sub.2 OMe Gc Q201 Ph SO.sub.2 Me G.sub.3 Q201 Ph SO.sub.2 NH.sub.2 Gc Q201 Ph SO.sub.2 NHMe Gc Q201 Ph SO.sub.2NMe.sub.2 G.sub.3 ______________________________________ TABLE 2 ______________________________________ ##STR25## A B D Gn ______________________________________ Q1 H COOMe Gb CH.sub.2 - Q1 H COOMe Gc CHMe - Q1 H COOMe G3 Q2 H COOMe Gb Q3 H COOMe Gb Q4 H COOMe Gb Q5 H COOMe Ga CH.sub.2 - Q5 H COOMe Gc CHMe - Q5 H COOMe G3 Q6 H COOMe G3 Q7 H COOMe G3 Q8 H COOMe G3 Q9 H COOMe Gc CH.sub.2 - Q9 H COOMe Gc Q10 H COOMe Gc Q11 H COOMe G3 Q12 H COOMe G3 Q13 H COOMe G3 Q14 H COOMe G1 Q15 H COOMe G3 Q16 H COOMe Gc Q17 H COOMe Gc Q18 HCOOMe G3 Q19 H COOMe Gc Q20 H COOMe Gc Q21 H COOMe Gc Q22 H COOMe G3 Q23 H COOMe Gc CH.sub.2 - Q23 H COOMe G3 Q24 H COOMe Gc Q25 H COOMe Gb Q26 H COOMe Ga CH.sub.2 - Q26 H COOMe G3 CHMe - Q26 H COOMe G3 Q27 H COOMe G3 Q28 H COOMe G3 Q29 HCOOMe Gc CH.sub.2 - Q29 H COOMe G3 Q30 H COOMe G3 Q31 H COOMe Gc Q32 H COOMe Gc CH.sub.2 - Q32 H COOMe G3 Q33 H COOMe G3 Q34 H COOMe G3 Q35 H COOMe G3 Q36 H COOMe G3 Q37 H COOMe Gc Q38 H COOMe Gc Q39 H COOMe G3 Q40 H COOMe Gc Q41 H COOMeGc Q42 H COOMe Gc Q43 H COOMe G3 Q44 H COOMe Gc Q45 H COOMe Gc Q46 H COOMe Gc Q47 H COOMe Gc Q48 H COOMe Gc Q49 H COOMe G3 Q50 H COOMe Gc CH.sub.2 - Q50 H COOMe G3 Q51 H COOMe Gc Q52 H COOMe G3 Q53 H COOMe G3 Q54 H COOMe Gc Q55 H COOMe Gc Q56 H COOMe Gc Q57 H COOMe G3 Q58 H COOMe Gc Q59 H COOMe Gc CH.sub.2 - Q59 H COOMe G3 Q60 H COOMe Gc Q61 H COOMe Ga CH.sub.2 - Q61 H COOMe Gb CHMe - Q61 H COOMe Gc Q62 H COOMe Gc Q63 H COOMe Gc Q64 H COOMe Gb CH.sub.2 - Q64 H COOMe G3 CHMe - Q64 H COOMe G3 Q65 H COOMe G3 Q66 H COOMe G3 Q67 H COOMe G3 Q68 H COOMe G3 Q69 H COOMe Gc Q70 H COOMe Gc Q71 H COOMe Gc Q72 H COOMe Gc CH.sub.2 - Q72 H COOMe G3 CHMe - Q72 H COOMe G3 Q73 H COOMe Gc CH.sub.2 - Q73 H COOMe G3 Q74 HCOOMe Gc Q75 H COOMe G3 Q76 H COOMe G3 Q77 H COOMe Gc CH.sub.2 - Q77 H COOMe G3 Q78 H COOMe Gc Q79 H COOMe Gc Q80 H COOMe Gc Q81 H COOMe G3 Q82 H COOMe G3 Q83 H COOMe G1 Q84 H COOMe G2 Q85 H COOMe G3 Q86 H COOMe Gc Q87 H COOMe G2 Q88 HCOOMe Gc Q89 H COOMe Gc Q90 H COOMe Gc Q91 H COOMe Gc Q92 H COOMe G3 Q93 H COOMe Gc Q94 H COOMe G3 Q95 H COOMe Gc Q96 H COOMe G3 Q97 H COOMe Gc Q98 H COOMe Gc Q99 H COOMe Gc Q100 H COOMe Gc Q101 H COOMe Gc CH.sub. 2 - Q101 H COOMe G3 Q102H COOMe G3 Q103 H COOMe G3 Q104 H COOMe G3 Q105 H COOMe Gc Q106 H COOMe G3 Q107 H COOMe Gc Q108 H COOMe G1 Q109 H COOMe G3 Q110 H COOMe G3 Q111 H COOMe G3 Q112 H COOMe Gc Q113 H COOMe Gc Q114 H COOMe Gc Q115 H COOMe G2 Q116 H COOMe Gc Q117H COOMe Gc Q118 H COOMe G3 Q119 H COOMe Gc Q120 H COOMe Gc Q121 H COOMe G2 Q122 H COOMe Gc Q123 H COOMe Gc Q124 H COOMe Gc Q125 H COOMe Gc Q126 H COOMe Gc Q127 H COOMe Gc Q128 H COOMe Gc Q129 H COOMe Gc Q130 H COOMe G2 Q131 H COOMe Gc Q132H COOMe Gc Q133 H COOMe G3 Q134 H COOMe G3 Q135 H COOMe Gc Q136 H COOMe G3 Q137 H COOMe G1 Q138 H COOMe Gc CH.sub.2 - Q138 H COOMe G3 Q139 H COOMe G3 Q140 H COOMe G1 Q141 H COOMe G3 Q142 H COOMe Gc Q143 H COOMe Gc CH.sub.2 - Q143 H COOMeG3 Q144 H COOMe G3 Q145 H COOMe Gc Q146 H COOMe Gc Q147 H COOMe G3 Q148 H COOMe G1 Q149 H COOMe G3 Q150 H COOMe G3 Q151 H COOMe G2 Q152 H COOMe G1 Q153 H COOMe Gc Q154 H COOMe Gc Q155 H COOMe G3 Q156 H COOMe G3 Q157 H COOMe Gc Q158 H COOMeGa CH.sub.2 - Q158 H COOMe G3 CHMe - Q158 H COOMe G3 Q159 H COOMe G3 Q160 H COOMe Gc Q161 H COOMe Gc Q162 H COOMe Gc Q163 H COOMe G3 Q164 H COOMe Gc Q165 H COOMe Gc Q166 H COOMe Gc Q167 H COOMe G3 Q168 H COOMe G3 Q169 H COOMe Gc CH.sub.2 -Q169 H COOMe G3 CHMe - Q169 H COOMe G3 Q170 H COOMe Gc Q171 H COOMe Gc Q172 H COOMe Gc Q173 H COOMe Gc Q174 H COOMe Gc Q175 H COOMe Gc Q176 H COOMe Gc Q177 H COOMe Gc CH.sub.2 - Q177 H COOMe G3 CHMe - Q177 H COOMe G3 Q178 H COOMe G3 Q179 HCOOMe G3 Q180 H COOMe Gc CH.sub.2 - Q180 H COOMe G3 Q181 H COOMe G1 Q182 H COOMe G3 Q183 H COOMe G3 Q184 H COOMe Gc CH.sub.2 - Q184 H COOMe G3 CHMe - Q184 H COOMe G3 Q185 H COOMe G3 Q186 H COOMe G3 Q187 H COOMe G3 Q188 H COOMe Gb Q189 HCOOMe Gb Q1 H COOEt Gb CH.sub.2 - Q1 H COOEt Gc CHMe - Q1 H COOEt G3 Q2 H COOEt Gb Q3 H COOEt Gb Q4 H COOEt Gb Q5 H COOEt Ga CH.sub.2 - Q5 H COOEt Gc CHMe - Q5 H COOEt G3 Q6 H COOEt G3 Q7 H COOEt G3 Q8 H COOEt G3 Q9 H COOEt Gc CH.sub.2 - Q9 H COOEt Gc Q10 H COOEt Gc Q11 H COOEtG3 Q12 H COOEt G3 Q13 H COOEt G3 Q14 H COOEt G1 Q15 H COOEt G3 Q16 H COOEt Gc Q17 H COOEt Gc Q18 H COOEt G3 Q19 H COOEt Gc Q20 H COOEt Gc Q21 H COOEt Gc Q22 H COOEt G3 Q23 H COOEt Gc CH.sub.2 - Q23 H COOEt G3 Q24 H COOEt Gc Q25 H COOEt Gb Q26 H COOEt Ga CH.sub.2 - Q26 H COOEt G3 CHMe - Q26 H COOEt G3 Q27 H COOEt G3 Q28 H COOEt G3 Q29 H COOEt Gc CH.sub.2 - Q29 H COOEt G3 Q30 H COOEt G3 Q31 H COOEt Gc Q32 H COOEt Gc CH.sub.2 - Q32 H COOEt G3 Q33 H COOEt G3 Q34 H COOEt G3 Q35H COOEt G3 Q36 H COOEt G3 Q37 H COOEt Gc Q38 H COOEt Gc Q39 H COOEt G3 Q40 H COOEt Gc Q41 H COOEt Gc Q42 H COOEt Gc Q43 H COOEt G3 Q44 H COOEt Gc Q45 H COOEt Gc Q46 H COOEt Gc Q47 H COOEt Gc Q48 H COOEt Gc Q49 H COOEt G3 Q50 H COOEt Gc CH.sub.2 - Q50 H COOEt G3 Q51 H COOEt Gc Q52 H COOEt G3 Q53 H COOEt G3 Q54 H COOEt Gc Q55 H COOEt Gc Q56 H COOEt Gc Q57 H COOEt G3 Q58 H COOEt Gc Q59 H COOEt Gc CH.sub.2 - Q59 H COOEt G3 Q60 H COOEt Gc Q61 H COOEt Ga CH.sub.2 - Q61 HCOOEt Gb CHMe - Q61 H COOEt Gc Q62 H COOEt Gc Q63 H COOEt Gc Q64 H COOEt Gb CH.sub. 2 - Q64 H COOEt G3 CHMe - Q64 H COOEt G3 Q65 H COOEt G3 Q66 H COOEt G3 Q67 H COOEt G3 Q68 H COOEt G3 Q69 H COOEt Gc Q70 H COOEt Gc Q71 H COOEt Gc Q72 HCOOEt Gc CH.sub.2 - Q72 H COOEt G3 CHMe - Q72 H COOEt G3 Q73 H COOEt Gc CH.sub.2 - Q73 H COOEt G3 Q74 H COOEt Gc Q75 H COOEt G3 Q76 H COOEt G3 Q77 H COOEt Gc CH.sub.2 - Q77 H COOEt G3 Q78 H COOEt Gc Q79 H COOEt Gc Q80 H COOEt Gc Q81 HCOOEt G3 Q82 H COOEt G3 Q83 H COOEt G1 Q84 H COOEt G2 Q85 H COOEt G3 Q86 H COOEt Gc Q87 H COOEt G2 Q88 H COOEt Gc Q89 H COOEt Gc Q90 H COOEt Gc Q91 H COOEt Gc Q92 H COOEt G3 Q93 H COOEt Gc Q94 H COOEt G3 Q95 H COOEt Gc Q96 H COOEt G3 Q97H COOEt Gc Q98 H COOEt Gc Q99 H COOEt Gc Q100 H COOEt Gc Q101 H COOEt Gc CH.sub.2 - Q101 H COOEt G3 Q102 H COOEt G3 Q103 H COOEt G3 Q104 H COOEt G3 Q105 H COOEt Gc Q106 H COOEt G3 Q107 H COOEt Gc Q108 H COOEt G1 Q109 H COOEt G3 Q110 HCOOEt G3 Q111 H COOEt G3 Q112 H COOEt Gc Q113 H COOEt Gc Q114 H COOEt Gc Q115 H COOEt G2 Q116 H COOEt Gc Q117 H COOEt Gc Q118 H COOEt G3 Q119 H COOEt Gc Q120 H COOEt Gc Q121 H COOEt G2 Q122 H COOEt Gc Q123 H COOEt Gc Q124 H COOEt Gc Q125 HCOOEt Gc Q126 H COOEt Gc Q127 H COOEt Gc Q128 H COOEt Gc Q129 H COOEt Gc Q130 H COOEt G2 Q131 H COOEt Gc Q132 H COOEt Gc Q133 H COOEt G3 Q134 H COOEt G3 Q135 H COOEt Gc Q136 H COOEt G3 Q137 H COOEt G1 Q138 H COOEt Gc CH.sub.2 - Q138 HCOOEt G3 Q139 H COOEt G3 Q140 H COOEt G1 Q141 H COOEt G3 Q142 H COOEt Gc Q143 H COOEt Gc CH.sub.2 - Q143 H COOEt G3 Q144 H COOEt G3 Q145 H COOEt Gc Q146 H COOEt Gc Q147 H COOEt G3 Q148 H COOEt G1 Q149 H COOEt G3 Q150 H COOEt G3 Q151 HCOOEt G2 Q152 H COOEt G1 Q153 H COOEt Gc Q154 H COOEt Gc Q155 H COOEt G3 Q156 H COOEt G3 Q157 H COOEt Gc Q158 H COOEt Ga CH.sub.2 - Q158 H COOEt G3 CHMe - Q158 H COOEt G3 Q159 H COOEt G3 Q160 H COOEt Gc Q161 H COOEt Gc Q162 H COOEt Gc Q163H COOEt G3 Q164 H COOEt Gc Q165 H COOEt Gc Q166 H COOEt Gc Q167 H COOEt G3 Q168 H COOEt G3 Q169 H COOEt Gc CH.sub.2 - Q169 H COOEt G3 CHMe - Q169 H COOEt G3 Q170 H COOEt Gc Q171 H COOEt Gc Q172 H COOEt Gc Q173 H COOEt Gc Q174 H COOEt Gc Q175 H COOEt Gc Q176 H COOEt Gc Q177 H COOEt Gc CH.sub.2 - Q177 H COOEt G3 CHMe - Q177 H COOEt G3 Q178 H COOEt G3 Q179 H COOEt G3 Q180 H COOEt Gc CH.sub.2 - Q180 H COOEt G3 Q181 H COOEt G1 Q182 H COOEt G3 Q183 H COOEt G3 Q184 H COOEt Gc CH.sub.2 - Q184 H COOEt G3 CHMe - Q184 H COOEt G3 Q185 H COOEt G3 Q186 H COOEt G3 Q187 H COOEt G3 Q188 H COOEt Gb Q189 H COOEt Gb Q5 H COOPri G3 Q26 H COOPri G3 Q61 H COOPri G3 Q158 H COOPri G3 Q5 H COOCH.sub.2 CH.sub.2 Cl G3 Q26 HCOOCH.sub.2 CH.sub.2 Cl G3 Q61 H COOCH.sub.2 CH.sub.2 Cl G3 Q158 H COOCH.sub.2 CH.sub.2 Cl G3 Q189 H COOCH.sub.2 CH.sub.2 Cl G3 Q5 H COOCH.sub.2 CHCH.sub.2 G3 Q26 H COOCH.sub.2 CHCH.sub.2 G3 Q61 H COOCH.sub.2 CHCH.sub.2 G3 Q158 H COOCH.sub.2 CHCH.sub.2 G3 Q5 H COOCH.sub.2 CCH G3 Q26 H COOCH.sub.2 CCH G3 Q61 HCOOCH.sub.2 CCH G3 Q158 H COOCH.sub.2 CCH G3 Q1 H COOPri G3 Q2 H COOCH.sub.2 CH.sub.2 Cl G3 Q4 H COOCH.sub.2 CHCH.sub.2 G3 Q7 H COOCH.sub.2 CCH G3 Q9 H COOPri G3 Q10 H COOCH.sub.2 CH.sub.2 Cl G3 Q19 H COOPri G3 Q23 H COOCH.sub.2 CHCH.sub.2 G3 Q32 H COOCH.sub.2 CCH G3 Q41 H COOPri G3 Q45 H COOCH.sub.2 CH.sub.2 Cl G3 Q50 H COOCH.sub.2 CCH G3 Q69 H COOPri G3 Q79 H COOCH.sub.2 CH.sub.2 Cl G3 Q83 H COOCH.sub.2 CCH G3 Q96 H COOPri G3 Q124 H COOCH.sub.2 CH.sub.2 Cl G3 Q131 HCOOCH.sub.2 CHCH.sub.2 G3 Q132 H COOCH.sub.2 CCH G3 Q135 H COOPri G3 Q138 H COOPri G3 Q142 H COOCH.sub.2 CHCH.sub.2 G3 Q157 H COOPri G3 Q159 H COOCH.sub.2 CH.sub.2 Cl G3 Q177 H COOCH.sub.2 CHCH.sub.2 G3 Q180 H COOCH.sub.2 CCH G3 Q184 HCOOPri G3 Q5 H COOH G3 Q26 H COOH G3 Q61 H COOH G3 Q158 H COOH G3 Q5 H CONHMe G3 Q26 H CONHMe G3 Q61 H CONHMe G3 Q158 H CONHMe G3 Q5 H CONMe.sub.2 G3 Q26 H CONMe.sub.2 G3 Q61 H CONMe.sub.2 G3 Q158 H CONMe.sub.2 G3 Q5 H COMe G3 Q26 H COMe G3 Q61 H COMe G3 Q188 H COMe Gb Q189 H COMe Gb Q158 H COMe G3 Q5 H COEt G3 Q26 H COEt G3 Q61 H COEt G3 Q158 H COEt G3 Q188 H COEt Gb Q189 H COEt Gb Q5 H COPri G3 Q26 H COPri G3 Q61 H COPri G3 Q158 H COPri G3 Q5 H COPh G3 Q26 H COPh G3 Q61 HCOPh G3 Q158 H COPh G3 Q1 H COMe G3 Q2 H COEt G3 Q4 H COMe G3 Q7 H COMe G3 Q9 H COEt G3 Q10 H COPri G3 Q19 H COPh G3 Q23 H COMe G3 Q32 H COMe G3 Q41 H COPri G3 Q45 H COPh G3 Q50 H COMe G3 Q69 H COEt G3 Q79 H COPri G3 Q83 H COPh G3 Q96 HCOMe G3 Q124 H COEt G3 Q131 H COMe G3 Q132 H COMe G3 Q135 H COEt G3 Q138 H COPri G3 Q142 H COPh G3 Q157 H COMe G3 Q159 H COEt G3 Q177 H COMe G3 Q180 H COMe G3 Q184 H COPri G3 Q4 H CN G3 Q5 H CN G3 Q7 H CN G3 Q9 H CN G3 Q23 H CN G3 Q26 HCN G3 Q32 H CN G3 Q61 H CN G3 Q96 H CN G3 Q142 H CN G3 Q158 H CN G3 Q5 H H G3 Q26 H H G3 Q61 H H G3 Q158 H H G3 Q5 H Me G3 Q26 H Me G3 Q61 H Me G3 Q158 H Me G3 Q5 H Et G3 Q26 H Et G3 Q61 H Et G3 Q158 H Et G3 Q5 H Pri G3 Q26 H Pri G3 Q61 H Pri G3 Q158 H Pri G3 Q5 H CHCH.sub.2 G3 Q26 H CHCH.sub.2 G3 Q61 H CHCHMe G3 Q158 H CHCHMe G3 Q5 H CH.sub.2 CHCH.sub.2 G3 Q26 H CH.sub.2 CHCH.sub.2 G3 Q61 H CH.sub.2 CHCH.sub.2 G3 Q158 H CH.sub.2 CHCH.sub.2 G3 Q1 H H G3 Q2 H Me G3 Q4H Me G3 Q7 H Me G3 Q9 H Et G3 Q10 H Pri G3 Q19 H Me G3 Q23 H CH.sub.2 CHCH.sub.2 G3 Q32 H H G3 Q41 H Me G3 Q45 H Me G3 Q50 H Et G3 Q69 H Pri G3 Q79 H Me G3 Q83 H Et G3 Q96 H Me G3 Q124 H Et G3 Q131 H Me G3 Q132 H CH.sub.2 CHCH.sub.2 G3 Q135 H Et G3 Q138 H Pri G3 Q142 H H G3 Q157 H Me G3 Q159 H Me G3 Q177 H H G3 Q180 H Me G3 Q184 H Me G3 Q5 H CH.sub.2 Cl G3 Q26 H CH.sub.2 Cl G3 Q61 H CH.sub.2 Cl G3 Q158 H CH.sub.2 Cl G3 Q5 H CH.sub.2 CH.sub.2 Cl G3 Q26 H CH.sub.2 CH.sub.2Cl G3 Q61 H CH.sub.2 CH.sub. 2 Cl G3 Q158 H CH.sub.2 CH.sub.2 Cl G3 Q5 H CF.sub.3 G3 Q26 H CF.sub.3 G3 Q61 H CF.sub.3 G3 Q158 H CF.sub.3 G3 Q5 H CFCFCl G3 Q26 H CFCFCl G3 Q61 H CH.sub.2 Ph G3 Q158 H CH.sub.2 Ph G3 Q5 H Ph G3 Q26 H Ph G3 Q61 H Ph G3 Q158 H Ph G3 Q5 H Ph2-Cl G3 Q26 H Ph2-Me G3 Q61 H Ph2-Cl G3 Q158 H Ph2-Me G3 Q1 H Ph G3 Q2 H CH.sub.2 Cl G3 Q4 H CH.sub.2 CH.sub.2 Cl G3 Q7 H Ph G3 Q9 H CF.sub.3 G3 Q10 H CF.sub.3 G3 Q19 H CFCFCl G3 Q23 H CH.sub.2 CH.sub.2 Cl G3 Q32 H Ph G3 Q41 H Ph2-Cl G3 Q45 H Ph2-Me G3 Q50 H CH.sub.2 CH.sub.2 Cl G3 Q69 H Ph G3 Q79 H CF.sub.3 G3 Q83 H CF.sub.3 G3 Q96 H Ph G3 Q124 H Ph2-Cl G3 Q131 H Ph2-Me G3 Q132 H CH.sub.2 CH.sub.2 Cl G3 Q135 H Ph G3 Q138 H CF.sub.3 G3 Q142H CF.sub.3 G3 Q157 H CFCFCl G3 Q159 H CH.sub.2 Cl G3 Q177 H CH.sub.2 CH.sub.2 Cl G3 Q180 H Ph G3 Q184 H Ph2-Cl G3 Q5 H Cl G3 Q26 H Cl G3 Q61 H Cl G3 Q158 H Cl G3 Q5 H Br G3 Q26 H Br G3 Q61 H Br G3 Q158 H Br G3 Q5 H F G3 Q26 H F G3 Q61 H I G3 Q158 H I G3 Q1 H Cl G3 Q2 H Cl G3 Q4 H Cl G3 Q7 H Br G3 Q9 H F G3 Q10 H I G3 Q19 H Cl G3 Q23 H Cl G3 Q32 H ClG3 Q41 H Br G3 Q45 H Br G3 Q50 H F G3 Q69 H Cl G3 Q79 H F G3 Q83 H Cl G3 Q96 H Cl G3 Q124 H Cl G3 Q131 H Br G3 Q132 H Br G3 Q135 H F G3 Q138 H Br G3 Q142 H Cl G3 Q157 H Cl G3 Q159 H Cl G3 Q177 H Br G3 Q180 H Br G3 Q184 H Cl G3 Q4 HNO.sub.2 G3 Q5 H NO.sub.2 G3 Q7 H NO.sub.2 G3 Q9 H NO.sub.2 G3 Q23 H NO.sub.2 G3 Q26 H NO.sub.2 G3 Q32 H NO.sub.2 G3 Q61 H NO.sub.2 G3 Q96 H NO.sub.2 G3 Q142 H NO.sub.2 G3 Q158 H NO.sub.2 G3 Q5 H NH.sub.2 G3 Q26 H NH.sub.2 G3 Q61 H NH.sub.2G3 Q158 H NH.sub.2 G3 Q5 H NHMe G3 Q26 H NHMe G3 Q61 H NHMe G3 Q158 H NHMe G3 Q5 H NMe.sub.2 G3 Q26 H NMe.sub.2 G3 Q61 H NMe.sub.2 G3 Q158 H NMe.sub.2 G3 Q5 H NMeEt G3 Q26 H NMeEt G3 Q61 H NMeEt G3 Q158 H NMeEt G3 Q5 H NHSO.sub.2 Me G3 Q26H NHSO.sub.2 Me G3 Q61 H NHSO.sub.2 Me G3 Q158 H NHSO.sub.2 Me G3 Q1 H NH.sub.2 G3 Q2 H NH.sub.2 G3 Q4 H NH.sub.2 G3 Q7 H NHMe G3 Q9 H NHMe G3 Q10 H NMe.sub.2 G3 Q19 H NMeEt G3 Q23 H NMe.sub.2 G3 Q32 H NMeEt G3 Q41 H NH.sub.2 G3 Q45 HNH.sub.2 G3 Q50 H NHMe G3 Q69 H NHMe G3 Q79 H NMe.sub.2 G3 Q83 H NMeEt G3 Q96 H NHSO.sub.2 Me G3 Q124 H NMe.sub.2 G3 Q131 H NMeEt G3 Q132 H NH.sub.2 G3 Q135 H NH.sub.2 G3 Q138 H NHMe G3 Q142 H NHMe G3 Q157 H NHSO.sub.2 Me G3 Q159 H NMe.sub.2G3 Q177 H NMeEt G3 Q180 H NH.sub.2 G3 Q184 H NH.sub.2 G3 Q4 H NHCOMe G3 Q5 H NHCOMe G3 Q7 H NHCOMe G3 Q9 H NHCOMe G3 Q23 H NHCOMe G3 Q26 H NHCOMe G3 Q32 H NHCOMe G3 Q61 H NHCOMe G3 Q96 H NHCOMe G3 Q142 H NHCOMe G3 Q158 H NHCOMe G3 Q5 H NHCOEt G3 Q26 H NHCOEt G3 Q61 H NHCOEt G3 Q158 H NHCOEt G3 Q5 H OMe G3 Q26 H OMe G3 Q61 H OMe G3 Q158 H OMe G3 Q5 H OEt G3 Q26 H OEt G3 Q61 H OEt G3 Q158 H OEt G3 Q5 H CH.sub.2 OMe G3 Q26 H CH.sub.2 OMe G3 Q61 H CH.sub.2 OMe G3 Q158 H CH.sub.2 OMe G3 Q5 H SMe G3 Q26 H SMe G3 Q61 H SMe G3 Q158 H SMe G3 Q5 H SO.sub.2 OMe G3 Q26 H SO.sub.2 OMe G3 Q61 HSO.sub.2 OMe G3 Q158 H SO.sub.2 OMe G3 Q1 H OMe G3 Q2 H OMe G3 Q4 H OEt G3 Q7 H SO.sub.2 OMe G3 Q9 H CH.sub.2 OMe G3 Q10 H SMe G3 Q19 H SO.sub.2 OMe G3 Q23 H OMe G3 Q32 H OEt G3 Q41 H SO.sub.2 OMe G3 Q45 H CH.sub.2 OMe G3 Q50 H SMe G3 Q69 HSO.sub.2 OMe G3 Q79 H OMe G3 Q83 H OEt G3 Q96 H CH.sub.2 OMe G3 Q124 H SMe G3 Q131 H OMe G3 Q132 H OEt G3 Q135 H CH.sub.2 OMe G3 Q138 H SMe G3 Q142 H SO.sub.2 OMe G3 Q157 H OMe G3 Q159 H OEt G3 Q177 H SO.sub.2 OMe G3 Q180 H OMe G3 Q184 HOEt G3 Q4 H SO.sub.2 Me G3 Q5 H SO.sub.2 Me G3 Q7 H SO.sub.2 Me G3 Q9 H SO.sub.2 Me G3 Q23 H SO.sub.2 Me G3 Q26 H SO.sub.2 Me G3 Q32 H SO.sub.2 Me G3 Q61 H SO.sub.2 Me G3 Q96 H SO.sub.2 Me G3 Q142 H SO.sub.2 Me G3 Q158 H SO.sub.2 Me G3 Q188 HSO.sub.2 Me Gb Q189 H SO.sub.2 Me Gb Q5 H SO.sub.2 Ph G3 Q26 H SO.sub.2 Ph G3 Q61 H SO.sub.2 Ph G3 Q158 H SO.sub.2 Ph G3 Q5 H SO.sub.2 NH.sub.2 G3 Q26 H SO.sub.2 NH.sub.2 G3 Q61 H SO.sub.2 NH.sub.2 G3 Q158 H SO.sub.2 NH.sub.2 G3 Q5 HSO.sub.2 NHMe G3 Q26 H SO.sub.2 NHMe G3 Q61 H SO.sub.2 NHMe G3 Q158 H SO.sub.2 NHMe G3 Q5 H SO.sub.2 NMe.sub.2 G3 Q26 H SO.sub.2 NMe.sub.2 G3 Q61 H SO.sub.2 NMe.sub.2 G3 Q158 H SO.sub.2 NMe.sub.2 G3 Q188 H SO.sub.2 NMe.sub.2 Gb Q189 HSO.sub.2 NMe.sub.2 Gb Q1 H SO.sub.2 Me G3 Q2 H SO.sub.2 Me G3 Q4 H SO.sub.2 Ph G3 Q7 H SO.sub.2 NH.sub.2 G3 Q9 H SO.sub.2 NH.sub.2 G3 Q10 H SO.sub.2 Ph G3 Q19 H SO.sub.2 Me G3 Q23 H SO.sub.2 Ph G3 Q32 H SO.sub. 2 NHMe G3 Q41 H SO.sub.2NMe.sub.2 G3 Q45 H SO.sub.2 Me G3 Q50 H SO.sub.2 NH.sub.2 G3 Q69 H SO.sub.2 Me G3 Q79 H SO.sub.2 Ph G3 Q83 H SO.sub.2 Me G3 Q96 H SO.sub.2 NMe.sub.2 G3 Q124 H SO.sub.2 NH.sub.2 G3 Q131 H SO.sub.2 Me G3 Q132 H SO.sub.2 Me G3 Q135 H SO.sub.2NHMe G3 Q138 H SO.sub.2 NMe.sub.2 G3 Q142 H SO.sub.2 NH.sub.2 G3 Q157 H SO.sub.2 Me G3 Q159 H SO.sub.2 Me G3 Q177 H SO.sub.2 NHMe G3 Q180 H SO.sub.2 NHMe.sub.2 G3 Q184 H SO.sub.2 Me G3 Q1 Me COOMe G3 Q2 Me COOMe G3 Q4 Me COOMe G3 Q5 MeCOOMe G3 Q7 Me COOMe G3 Q9 Me COOMe G3 Q10 Me COOMe G3 Q19 Me COOMe G3 Q23 Me COOMe G3 Q26 Me COOMe G3 Q32 Me COOMe G3 Q41 Me COOMe G3 Q45 Me COOMe G3 Q50 Me COOMe G3 Q61 Me COOMe G3 Q69 Me COOMe G3 Q79 Me COOMe G3 Q83 Me COOMe G3 Q96 MeCOOMe G3 Q124 Me COOMe G3 Q131 Me COOMe G3 Q132 Me COOMe G3 Q135 Me COOMe G3 Q138 Me COOMe G3 Q142 Me COOMe G3 Q157 Me COOMe G3 Q158 Me COOMe G3 Q159 Me COOMe G3 Q177 Me COOMe G3 Q180 Me COOMe G3 Q184 Me COOMe G3 Q1 Me COOEt G3 Q2 Me COOEtG3 Q4 Me COOEt G3 Q5 Me COOEt G3 Q7 Me COOEt G3 Q9 Me COOEt G3 Q10 Me COOEt G3 Q19 Me COOEt G3 Q23 Me COOEt G3 Q26 Me COOEt G3 Q32 Me COOEt G3 Q41 Me COOEt G3 Q45 Me COOEt G3 Q50 Me COOEt G3 Q61 H COOEt G3 Q69 Me COOEt G3 Q79 Me COOEt G3 Q83 Me COOEt G3 Q96 Me COOEt G3 Q124 Me COOEt G3 Q131 Me COOEt G3 Q132 Me COOEt G3 Q135 Me COOEt G3 Q138 Me COOEt G3 Q142 Me COOEt G3 Q157 Me COOEt G3 Q158 Me COOEt G3 Q159 Me COOEt G3 Q177 Me COOEt G3 Q180 Me COOEt G3 Q184 Me COOEt G3 Q158Me COOEt G3 Q5 Me COOPri G3 Q26 Me COOPri G3 Q61 Me COOPri G3 Q158 Me COOPri G3 Q5 Me COOCH.sub.2 CH.sub.2 Cl G3 Q26 Me COOCH.sub.2 CH.sub.2 Cl G3 Q61 Me COOCH.sub.2 CH.sub.2 Cl G3 Q158 Me COOCH.sub.2 CH.sub.2 Cl G3 Q5 Me COOCH.sub.2CHCH.sub.2 G3 Q26 Me COOCH.sub.2 CHCH.sub.2 G3 Q61 Me COOCH.sub.2 CHCH.sub.2 G3 Q158 Me COOCH.sub.2 CHCH.sub.2 G3 Q5 Me COOCH.sub.2 CCH G3 Q26 Me COOCH.sub.2 CCH G3 Q61 Me COOCH.sub.2 CCH G3 Q158 Me COOCH.sub.2 CCH G3 Q5 Me CONHMe G3 Q26Me CONHMe G3 Q61 Me CONHMe G3 Q158 Me CONHMe G3 Q5 Me CONMe.sub.2 G3 Q26 Me CONMe.sub.2 G3 Q61 Me CONMe.sub.2 G3 Q158 Me CONMe.sub.2 G3 Q1 Me COOPri G3 Q2 Me COOPri G3 Q4 Me COOCH.sub.2 CH.sub.2 Cl G3 Q7 Me COOCH.sub.2 CHCH.sub.2 G3 Q9 MeCOOCH.sub.2 CCH G3 Q10 Me COOCH.sub.2 CH.sub.2 Cl G3 Q19 Me COOPri G3 Q23 Me COOCH.sub.2 CH.sub.2 Cl G3 Q32 Me CONMe.sub.2 G3 Q41 Me COOPri G3 Q45 Me CONHMe G3 Q50 Me CONMe.sub.2 G3 Q69 Me COOCH.sub.2 CH.sub.2 Cl G3 Q79 Me COOCH.sub.2 CHCH.sub.2 G3 Q83 Me COOPri G3 Q96 Me COOCH.sub.2 CH.sub.2 Cl G3 Q124 Me COOPri G3 Q131 Me COOCH.sub.2 CH.sub.2 Cl G3 Q132 Me CONHMe G3 Q135 Me CONMe.sub.2 G3 Q138 Me COOCH.sub.2CCH G3 Q142 Me COOPri G3 Q157 Me COOPri G3 Q159 Me COOCH.sub.2 CHCH.sub.2 G3 Q177 Me COOCH.sub.2 CCH G3 Q180 Me COOPri G3 Q184 Me COOCH.sub.2 CH.sub.2 Cl G3 Q5 Me COMe G3 Q26 Me COMe G3 Q61 Me COMe G3 Q158 Me COMe G3 Q5 Me COEt G3 Q26 MeCOEt G3 Q61 Me COEt G3 Q158 Me COEt G3 Q5 Me COPri G3 Q26 Me COPri G3 Q61 Me COPri G3 Q158 Me COPr i G3 Q5 Me CN G3 Q26 Me CN G3 Q61 Me CN G3 Q158 Me CN G3 Q5 Me H G3 Q26 Me H G3 Q61 Me H G3 Q158 Me H G3 Q5 Me Me G3 Q26 Me Me G3 Q61 MeMe G3 Q158 Me Me G3 Q5 Me Et G3 Q26 Me Et G3 Q61 Me Et G3 Q158 Me Et G3 Q5 Me Pri G3 Q26 Me Pri G3 Q61 Me CHCH.sub.2 G3 Q158 Me CHCH.sub.2 G3 Q5 Me CHCHMe G3 Q26 Me CH.sub.2 CHCH.sub.2 G3 Q61 Me CHCHMe G3 Q158 Me CH.sub.2 CHCH.sub.2 G3 Q1Me COMe G3 Q2 Me COEt G3 Q4 Me CHCHMe G3 Q7 Me CH.sub.2 CHCH.sub.2 G3 Q9 Me CN G3 Q10 Me H G3 Q19 Me Me G3 Q23 Me COMe G3 Q32 Me COEt G3 Q41 Me H G3 Q45 Me Me G3 Q50 Me COPri G3 Q69 Me CN G3 Q79 Me Et G3 Q83 Me Pri G3 Q96 Me COMe G3 Q124Me COEt G3 Q131 Me CH.sub.2 CHCH.sub.2 G3 Q132 Me Me G3 Q135 Me COPr-i G3 Q138 Me CN G3 Q142 Me Et G3 Q157 Me CH.sub.2 CHCH.sub.2 G3 Q159 Me COMe G3 Q177 Me COEt G3 Q180 Me CHCHMe G3 Q184 Me COMe G3 Q5 Me CH.sub.2 Cl G3 Q26 Me CH.sub.2 ClG3 Q5 Me CH.sub.2 CH.sub.2 Cl G3 Q26 Me CH.sub.2 CH.sub.2 Cl G3 Q61 Me CH.sub.2 CH.sub.2 Cl G3 Q158 Me CH.sub.2 CH.sub.2 Cl G3 Q5 Me CF.sub.3 G3 Q26 Me CF.sub.3 G3 Q61 Me CF.sub.3 G3 Q158 Me CF.sub.3 G3 Q5 Me CFCFCl G3 Q26 Me CFCFCl G3 Q61Me CH.sub.2 Ph G3 Q158 Me CH.sub.2 Ph G3 Q5 Me Ph G3 Q26 Me Ph G3 Q61 Me Ph G3 Q158 Me Ph G3 Q5 Me Ph2-Cl G3 Q26 Me Ph2-Cl G3 Q61 Me Ph2-Me G3 Q158 Me Ph2-Me G3 Q5 Me Cl G3 Q26 Me Cl G3 Q61 Me Cl G3 Q158 Me Cl G3 Q5 Me Br G3 Q26 Me Br G3 Q61 Me Br G3 Q158 Me Br G3 Q5 Me F G3 Q26 Me F G3 Q61 Me I G3 Q158 Me I G3 Q1 Me Ph G3 Q2 Me Cl G3 Q4 Me CH.sub.2 CH.sub.2 Cl G3 Q7 Me Ph G3 Q9 Me Ph G3 Q10 Me Cl G3 Q19 Me Cl G3 Q23 Me Br G3 Q32 Me CH.sub.2 Cl G3 Q41 Me CH.sub.2 CH.sub.2Cl G3 Q45 Me CF.sub.3 G3 Q50 Me Cl G3 Q69 Me Cl G3 Q79 Me Br G3 Q83 Me Ph G3 Q96 Me CF.sub.3 G3 Q124 Me CF.sub.3 G3 Q131 Me CH.sub.2 CH.sub.2 Cl G3 Q132 Me Ph G3 Q135 Me Br G3 Q138 Me Ph G3 Q142 Me Ph G3 Q157 Me Cl G3 Q159 Me Br G3 Q177Me CF.sub.3 G3 Q180 Me CH.sub.2 CH.sub.2 Cl G3 Q184 Me Ph G3 Q5 Me NO.sub.2 G3 Q26 Me NO.sub.2 G3 Q61 Me NO.sub.2 G3 Q158 Me NO.sub.2 G3 Q5 Me NH.sub.2 G3 Q26 Me NH.sub.2 G3 Q61 Me NH.sub.2 G3 Q158 Me NH.sub.2 G3 Q5 Me NHMe G3 Q26 Me NHMe G3 Q61 Me NHMe G3 Q158 Me NHMe G3 Q5 Me NMe.sub.2 G3 Q26 Me NMe.sub.2 G3 Q61 Me NMe.sub.2 G3 Q158 Me NMe.sub.2 G3 Q5 Me NMeEt G3 Q26 Me NMeEt G3 Q5 Me NHCOMe G3 Q26 Me NHCOMe G3 Q61 Me NHCOMe G3 Q158 Me NHCOMe G3 Q5 Me NHCOEt G3 Q26 Me NHCOEtG3 Q61 Me NHSO.sub.2 Me G3 Q158 Me NHSO.sub.2 Me G3 Q5 Me OMe G3 Q26 Me OMe G3 Q61 Me OMe G3 Q158 Me OMe G3 Q5 Me OEt G3 Q26 Me OEt G3 Q61 Me CH.sub.2 OMe G3 Q158 Me CH.sub.2 OMe G3 Q1 Me NO.sub.2 G3 Q2 Me NHCOMe G3 Q4 Me NHCOEt G3 Q7 MeNHMe G3 Q9 Me NO.sub.2 G3 Q10 Me NH.sub.2 G3 Q19 Me NHCOMe G3 Q23 Me OMe G3 Q32 Me NHCOMe G3 Q41 Me NHCOEt G3 Q45 Me CH.sub.2 OMe G3 Q50 Me OMe G3 Q69 Me OEt G3 Q79 Me NO.sub.2 G3 Q83 Me NH.sub.2 G3 Q96 Me NMe.sub.2 G3 Q124 Me NMeEt G3 Q131Me NHCOMe G3 Q132 Me NHCOEt G3 Q135 Me NO.sub.2 G3 Q138 Me OMe G3 Q142 Me OEt G3 Q157 Me NO.sub.2 G3 Q159 Me NH.sub.2 G3 Q177 Me OMe G3 Q180 Me NHCOMe G3 Q184 Me NO.sub.2 G3 Q26 Me SMe G3 Q61 Me SMe G3 Q5 Me SO.sub.2 Me G3 Q26 Me SO.sub.2 MeG3 Q61 Me SO.sub.2 Me G3 Q158 Me SO.sub.2 Me G3 Q5 Me SO.sub.2 Ph G3 Q26 Me SO.sub.2 Ph G3 Q61 Me SO.sub.2 Ph G3 Q158 Me SO.sub.2 Ph G3 Q5 Me SO.sub.2 OMe G3 Q26 Me SO.sub.2 OMe G3 Q61 Me SO.sub.2 NH.sub.2 G3 Q158 Me SO.sub.2 NH.sub.2 G3 Q5Me SO.sub.2 NMe G3 Q26 Me SO.sub.2 NMe G3 Q61 Me SO.sub.2 NMe G3 Q158 Me SO.sub.2 NMe G3 Q5 Me SO.sub.2 NHMe.sub.2 G3 Q26 Me SO.sub.2 NHMe.sub.2 G3 Q61 Me SO.sub.2 NHMe.sub.2 G3 Q158 Me SO.sub.2 NHMe.sub.2 G3 Q1 Me SO.sub.2 Ph G3 Q2 MeSO.sub.2 OMe G3 Q4 Me SO.sub.2 NHMe G3 Q7 Me SO.sub.2 NMe.sub.2 G3 Q9 Me SO.sub.2 Me G3 Q10 Me SO.sub.2 Me G3 Q19 Me SMe G3 Q23 Me SO.sub.2 Me G3 Q32 Me SO.sub.2 OMe G3 Q41 Me SO.sub.2 NMe.sub.2 G3 Q45 Me SO.sub.2 NHMe G3 Q50 Me SO.sub.2 NMe.sub.2 G3 Q69 Me SO.sub.2 Me G3 Q79 Me SO.sub.2 Me G3 Q83 Me SO.sub.2 Ph G3 Q96 Me SO.sub.2 OMe G3 Q124 Me SO.sub.2 NMe.sub.2 G3 Q131 Me SO.sub.2 NHMe G3 Q132 Me SO.sub.2 NMe.sub.2 G3 Q135 Me SO.sub.2 Ph G3 Q138 Me SO.sub.2 Ph G3 Q142 Me SO.sub.2 Me G3 Q157 Me SO.sub.2 Me G3 Q159 Me SO.sub.2 NHMe G3 Q177 Me SO.sub.2 NMe.sub.2 G3 Q180 Me SO.sub.2 NMe.sub.2 G3 Q184 Me SO.sub.2 Me.sub.2 G3 Q5 Et COOMe G3 Q26 Et COOMe G3 Q61 Et COOMe G3 Q142 Et COOMe G3 Q158 Et COOMe G3 Q159 Et COOMe G3 Q4 EtCOOEt G3 Q5 Et COOEt G3 Q9 Et COOEt G3 Q26 Et COOEt G3 Q32 Et COOEt G3 Q61 Et COOEt G3 Q69 Et COOEt G3 Q96 Et COOEt G3 Q158 Et COOEt G3 Q61 Et COOPri G3 Q158 Et COOPri G3 Q5 Et COOCH.sub.2 CH.sub.2 Cl G3 Q26 Et COOCH.sub.2 CH.sub.2 Cl G3 Q5 Et COOCH.sub.2 CHCH.sub.2 G3 Q158 Et COOCH.sub.2 CHCH.sub.2 G3 Q5 Et COOCH.sub.2 CCH G3 Q26 Et COOCH.sub.2 CCH G3 Q5 Et CONHMe G3 Q26 Et CONMe.sub.2 G3 Q1 Et COOPri G3 Q4 Et COOCH.sub.2 CH.sub.2 Cl G3 Q69 Et COOCH.sub.2 CH.sub.2 Cl G3 Q79 Et COOCH.sub.2 CHCH.sub.2 G3 Q83 Et COOPri G3 Q96 Et COOCH.sub.2 CH.sub.2 Cl G3 Q131 Et COOCH.sub.2 CH.sub.2 Cl G3 Q157 Et COOPri G3 Q159 Et COOCH.sub.2 CHCH.sub.2 G3 Q184 Et COOCH.sub.2 CH.sub.2 Cl G3 Q5 Et COMe G3 Q26 Et COMe G3 Q158Et COEt G3 Q5 Et COPri G3 Q26 Et CN G3 Q61 Et H G3 Q26 Et Me G3 Q158 Et Et G3 Q5 Et Pri G3 Q1 Et COMe G3 Q2 Et COEt G3 Q9 Et CN G3 Q23 Et COMe G3 Q96 Et COMe G3 Q124 Et COEt G3 Q135 Et COPri G3 Q138 Et CN G3 Q5 Et CH.sub.2 CH.sub.2 Cl G3 Q26 Et CH.sub.2 CH.sub.2 Cl G3 Q158 Et CF.sub.3 G3 Q5 Et Ph G3 Q26 Et Ph G3 Q158 Et Ph2-Me G3 Q26 Et Cl G3 Q61 Et Cl G3 Q5 Et Br G3 Q1 Et Ph G3 Q2 Et Cl G3 Q9 Et Ph G3 Q5 Et NO.sub.2 G3 Q5 Et NH.sub.2 G3 Q5 Et NHMe G3 Q26 Et NMe.sub.2 G3 Q61 Et NHCOMe G3 Q158 Et NHSO.sub.2 Me G3 Q2 Et NHCOMe G3 Q23 Et OMe G3 Q32 Et NHCOMe G3 Q96 Et NMe.sub.2 G3 Q26 Et SO.sub.2 Me G3 Q61 Et SO.sub.2 Me G3 Q5 Et SO.sub.2 Ph G3 Q26 Et SO.sub.2 OMe G3 Q61 Et SO.sub.2 NH.sub.2 G3 Q5 Et SO.sub.2NHMe G3 Q26 Et SO.sub.2 NMe.sub.2 G3 Q4 Et SO.sub.2 NHMe G3 Q7 Et SO.sub.2 NMe.sub.2 G3 Q9 Et SO.sub.2 Me G3 Q142 Et SO.sub.2 Me G3 Q159 Et SO.sub.2 NMe.sub.2 G3 Q5 Cl COOMe G3 Q26 Cl COOMe G3 Q61 Cl COOMe G3 Q5 Cl COOEt G3 Q26 Cl COOEt G3 Q61 Cl COOEt G3 Q96 Cl COOEt G3 Q158 Cl COOEt G3 Q61 Cl COOPri G3 Q5 Cl COMe G3 Q158 Cl COEt G3 Q5 Cl COPri G3 Q26 Cl CN G3 Q61 Cl H G3 Q26 Cl Me G3 Q158 Cl Et G3 Q5 Cl Pri G3 Q1 Cl COMe G3 Q26 Cl CH.sub.2 CH.sub.2 Cl G3 Q158 Cl CF.sub.3G3 Q5 Cl Ph G3 Q26 Cl Cl G3 Q5 Cl Br G3 Q2 Cl Cl G3 Q9 Cl Ph G3 Q5 Cl NO.sub.2 G3 Q5 Cl NH.sub.2 G3 Q5 Cl NHMe G3 Q26 Cl NMe.sub.2 G3 Q61 Cl NHCOMe G3 Q158 Cl NHSO.sub.2 Me G3 Q2 Cl NHCOMe G3 Q26 Cl SO.sub.2 Me G3 Q61 Cl SO.sub.2 Me G3 Q5Cl SO.sub.2 Ph G3 Q61 Cl SO.sub.2 NH.sub.2 G3 Q5 Cl SO.sub.2 NHMe G3 Q26 Cl SO.sub.2 NMe.sub.2 G3 Q5 Br COOMe G3 Q26 Br COOMe G3 Q61 Br COOMe G3 Q5 Br COOEt G3 Q26 Br COOEt G3 Q61 Br COOEt G3 Q61 Br COOPri G3 Q5 Br COMe G3 Q158 Br COEt G3 Q26 Br CN G3 Q26 Br Me G3 Q158 Br Et G3 Q26 Br CH.sub.2 CH.sub.2 Cl G3 Q158 Br CF.sub.3 G3 Q5 Br Ph G3 Q26 Br Cl G3 Q5 Br Br G3 Q5 Br NO.sub.2 G3 Q5 Br NH.sub.2 G3 Q26 Br NMe.sub.2 G3 Q61 Br NHCOMe G3 Q61 Br SO.sub.2 Me G3 Q5 Br SO.sub.2 PhG3 Q61 Br SO.sub.2 NH.sub.2 G3 Q26 Br SO.sub.2 NMe.sub.2 G3 Q5 SMe COOMe G3 Q26 SMe COOMe G3 Q61 SMe COOMe G3 Q5 SMe COOEt G3 Q26 SMe COOEt G3 Q61 SMe COOEt G3 Q61 SMe COOPri G3 Q5 SMe COMe G3 Q158 SMe COEt G3 Q26 SMe CN G3 Q26 SMe Me G3 Q158 SMe Et G3 Q26 SMe CH.sub.2 CH.sub.2 Cl G3 Q158 SMe CF.sub.3 G3 Q5 SMe Ph G3 Q26 SMe Cl G3 Q5 SMe Br G3 Q5 SMe NO.sub.2 G3 Q5 SMe NH.sub.2 G3 Q26 SMe NMe.sub.2 G3 Q61 SMe NHCOMe G3 Q61 SMe SO.sub.2 Me G3 Q5 SMe SO.sub.2 Ph G3 Q61 SMeSO.sub.2 NH.sub.2 G3 Q26 SMe SO.sub.2 NMe.sub.2 G3 Q5 SO.sub. 2 Me COOMe G3 Q26 SO.sub.2 Me COOMe G3 Q61 SO.sub.2 Me COOMe G3 Q5 SO.sub.2 Me COOEt G3 Q26 SO.sub.2 Me COOEt G3 Q61 SO.sub.2 Me COOEt G3 Q96 SO.sub.2 Me COOEt G3 Q158SO.sub.2 Me COOEt G3 Q61 SO.sub.2 Me COOPri G3 Q5 SO.sub.2 Me COMe G3 Q158 SO.sub.2 Me COEt G3 Q5 SO.sub.2 Me COPri G3 Q26 SO.sub.2 Me CN G3 Q61 SO.sub.2 Me H G3 Q26 SO.sub.2 Me Me G3 Q158 SO.sub.2 Me Et G3 Q5 SO.sub.2 Me Pri G3 Q1 SO.sub.2 Me COMeG3 Q26 SO.sub.2 Me CH.sub.2 CH.sub.2 Cl G3 Q158 SO.sub.2 Me CF.sub.3 G3 Q5 SO.sub.2 Me Ph G3 Q26 SO.sub.2 Me Cl G3 Q5 SO.sub.2 Me Br G3 Q2 SO.sub.2 Me Cl G3 Q9 SO.sub.2 Me Ph G3 Q5 SO.sub.2 Me NO.sub.2 G3 Q5 SO.sub.2 Me NH.sub.2 G3 Q5SO.sub.2 Me NHMe G3 Q26 SO.sub.2 Me NMe.sub.2 G3 Q61 SO.sub.2 Me NHCOMe G3 Q158 SO.sub.2 Me NHSO.sub.2 Me G3 Q2 SO.sub.2 Me NHCOMe G3 Q26 SO.sub.2 Me SO.sub.2 Me G3 Q61 SO.sub.2 Me SO.sub.2 Me G3 Q5 SO.sub.2 Me SO.sub.2 Ph G3 Q61 SO.sub.2Me SO.sub.2 NH.sub.2 G3 Q5 SO.sub.2 Me SO.sub.2 NHMe G3 Q26 SO.sub.2 Me SO.sub.2 NMe.sub.2 G3 Q5 Ph COOMe G3 Q26 Ph COOMe G3 Q61 Ph COOMe G3 Q5 Ph COOEt G3 Q26 Ph COOEt G3 Q61 Ph COOEt G3 Q61 Ph COOPri G3 Q5 Ph COMe G3 Q158 Ph COEt G3 Q26 Ph CN G3 Q26 Ph Me G3 Q158 Ph Et G3 Q26 Ph CH.sub.2 CH.sub.2 Cl G3 Q158 Ph CF.sub.3 G3 Q5 Ph Ph G3 Q26 Ph Cl G3 Q5 Ph Br G3 Q5 Ph NO.sub.2 G3 Q5 Ph NH.sub.2 G3 Q26 Ph NMe.sub.2 G3 Q61 Ph NHCOMe G3 Q61 Ph SO.sub.2 Me G3 Q5 Ph SO.sub.2 PhG3 Q61 Ph SO.sub.2 NH.sub.2 G3 Q26 Ph SO.sub.2 NMe.sub.2 G3 Q201 H COOMe Ga CH.sub.2 - Q201 H COOMe Gb CHMe - Q201 H COOMe Gb Q202 H COOMe Gb CH.sub.2 - Q202 H COOMe Gb Q203 H COOMe Gb Q204 H COOMe Gb Q205 H COOMe Gb CH.sub.2 - Q205 H COOMe Gc Q206 H COOMe G.sub.3 Q207 H COOMe Gc Q208 H COOMe G.sub.3 Q209 H COOMe Gc CH.sub.2 - Q209 H COOMe Gc Q210 H COOMe Gc CH.sub.2 - Q210 H COOMe G.sub.3 Q211 H COOMe G.sub.3 Q212 H COOMe Gc Q213 H COOMe Gc Q214 H COOMe Gc Q215 H COOMe G.sub.1 Q216 H COOMe Gc Q217 H COOMe Gc Q218 H COOMe G.sub.3 Q219 H COOMe Gc Q220 H COOMe Gc Q221 H COOMe G.sub.2 Q222 H COOMe Gb CH.sub.2 - Q222 H COOMe Gc Q223 H COOMe Gc Q224 H COOMe G.sub.3 Q225 H COOMe Gb CH.sub.2 - Q225 H COOMe Gc Q226 H COOMe G.sub.3 Q227 H COOMe Gc Q228 H COOMe Gc Q229 H COOMe Gb CH.sub.2 - Q229 H COOMe Gc Q230 H COOMe Gc Q231 H COOMe Gc Q232 H COOMe G.sub.3 Q233 H COOMe Gc Q234 H COOMe Gc Q235 H COOMe Gc Q236 H COOMeG.sub.3 Q237 H COOMe Gc Q238 H COOMe Gc Q239 H COOMe G.sub.2 Q240 H COOMe Gc Q241 H COOMe Gc Q242 H COOMe Gc Q243 H COOMe G.sub.1 Q244 H COOMe Gc Q245 H COOMe Gc Q246 H COOMe Gb CH.sub.2 - Q246 H COOMe Gc Q247 H COOMe G.sub.3 Q248 H COOMeGc Q249 H COOMe Gc Q250 H COOMe Gc CH.sub.2 - Q250 H COOMe G.sub.3 Q251 H COOMe Gc Q252 H COOMe Gc Q253 H COOMe Gc Q254 H COOMe G.sub.1 Q255 H COOMe Gc Q256 H COOMe Gc Q257 H COOMe G.sub.3 Q258 H COOMe Gc Q259 H COOMe Gc CH.sub.2 - Q259 HCOOMe Gc Q260 H COOMe Gc CH.sub.2 - Q260 H COOMe Gc Q261 H COOMe G.sub.1 Q262 H COOMe Gc Q263 H COOMe Gc Q264 H COOMe G.sub.2 Q201 H COOEt Ga CH.sub.2 - Q201 H COOEt Gb CHMe - Q201 H COOEt Gb Q202 H COOEt Gb CH.sub.2 - Q202 H COOEt Gb Q203H COOEt Gb Q204 H COOEt Gb Q205 H COOEt Gb CH.sub.2 - Q205 H COOEt Gc Q206 H COOEt G.sub.3 Q207 H COOEt Gc Q208 H COOEt G.sub.3 Q209 H COOEt Gc CH.sub.2 - Q209 H COOEt Gc Q210 H COOEt Gc CH.sub.2 - 210 H COOEt G.sub.3 Q211 H COOEt Gc Q212H COOEt Gc Q213 H COOEt Gc Q214 H COOEt G.sub.1 Q215 H COOEt Gc Q216 H COOEt Gc Q217 H COOEt G.sub.2 Q218 H COOEt Gc Q219 H COOEt Gc Q220 H COOEt G.sub.3 Q221 H COOEt Gc Q222 H COOEt Gb CH.sub.2 - Q222 H COOEt Gc Q223 H COOEt Gc Q224 HCOOEt Gc Q225 H COOEt Gb CH.sub.2 - Q225 H COOEt Gc Q226 H COOEt G.sub.3 Q227 H COOEt Gc Q228 H COOEt Gc Q229 H COOEt Gb CH.sub.2 - Q229 H COOEt Gc Q230 H COOEt Gc Q231 H COOEt Gc Q232 H COOEt G.sub.3 Q233 H COOEt Gc Q234 H COOEt Gc CH.sub.2 - Q234 H COOEt Gc Q235 H COOEt Gc Q236 H COOEt G.sub.3 Q237 H COOEt Gc Q238 H COOEt Gc Q239 H COOEt Gc Q240 H COOEt G.sub.1 Q241 H COOEt Gc Q242 H COOEt Gc Q243 H COOEt Gc Q244 H COOEt G.sub.2 Q245 H COOEt Gc Q246 H COOEt Gb CH.sub.2 - Q246 H COOEt Gc Q247 H COOEt Gc Q248 H COOEt Gc Q249 H COOEt G.sub.3 Q250 H COOEt Gc CH.sub.2 - Q250 H COOEt Gc Q251 H COOEt Gc Q252 H COOEt G.sub.3 Q253 H COOEt Gc Q254 H COOEt Gc Q255 H COOEt Gc Q256 H COOEt Gc Q257 H COOEt Gc Q258 H COOEt G.sub.1 Q259 H COOEt Gc CH.sub.2 - Q259 H COOEt Gc Q260 H COOEt Gc CH.sub.2 - Q260 H COOEt Gc Q261 H COOEt G.sub.3 Q262 H COOEt Gc Q263 H COOEt Gc Q264 H COOEt G.sub.3 Q201 H COOH Gc Q202 H COOH Gc Q222 H COOH Gc Q225 H COOHG.sub.3 Q229 H COOH Gc Q246 H COOH G.sub.3 Q201 H COOPri Gc Q202 H COOPri G.sub.3 Q205 H COOPri Gc Q209 H COOPri Gc Q222 H COOPri Gc Q225 H COOPri Gc Q229 H COOPri G.sub.3 Q246 H COOPri Gc Q201 H COOCH.sub.2 CH.sub.2 Cl Gc Q202 H COOCH.sub.2CH.sub.2 Cl G.sub.3 Q205 H COOCH.sub.2 CH.sub.2 Cl Gc Q209 H COOCH.sub.2 CH.sub.2 Cl Gc Q222 H COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q225 H COOCH.sub.2 CH.sub.2 Cl Gc Q229 H COOCH.sub.2 CH.sub.2 Cl Gc Q246 H COOCH.sub.2 CH.sub.2 Cl G.sub.1 Q201 HCOOCH.sub.2 CHCH.sub.2 Gc Q202 H COOCH.sub.2 CHCH.sub.2 Gc Q205 H COOCH.sub.2 CHCH.sub.2 G.sub.3 Q209 H COOCH.sub.2 CHCH.sub.2 Gc Q222 H COOCH.sub.2 CHCH.sub.2 Gc Q225 H COOCH.sub.2 CHCH.sub.2 Gc Q229 H COOCH.sub.2 CHCH.sub.2 G.sub.3 Q246 HCOOCH.sub.2 CHCH.sub.2 Gc Q201 H COOCH.sub.2 CCH Gc Q202 H COOCH.sub.2 CCH G.sub.3 Q205 H COOCH.sub.2 CCH Gc Q209 H COOCH.sub.2 CCH Gc Q222 H COOCH.sub. 2 CCH Gc Q225 H COOCH.sub.2 CCH G.sub.3 Q229 H COOCH.sub.2 CCH Gc Q246 H COOCH.sub.2CCH G.sub.3 Q201 H CONHMe Gc Q202 H CONHMe G.sub.3 Q205 H CONHMe Gc Q209 H CONHMe Gc Q222 H CONHMe G.sub.3 Q225 H CONHMe Gc Q229 H CONHMe Gc Q246 H CONHMe G.sub.3 Q201 H CONMe.sub.2 Gc Q202 H CONMe.sub.2 G.sub.3 Q205 H CONMe.sub.2 Gc Q209 HCONMe.sub.2 Gc Q222 H CONMe.sub.2 Gc Q225 H COMe Gc Q229 H COMe Gc Q230 H COMe G.sub.2 Q231 H COMe G.sub.3 Q237 H COMe Gc Q246 H COMe Gc Q247 H COMe G.sub.3 Q250 H COMe Gc Q259 H COMe Gc Q260 H COMe Gc Q263 H COMe G.sub.3 Q201 H COEt Gc Q202 H COEt G.sub.3 Q205 H COEt Gc Q209 H COEt Gc Q222 H COEt Gc Q225 H COEt G.sub.3 Q229 H COEt Gc Q246 H COEt G.sub.3 Q201 H COPriGc Q202 H COPri G.sub.3 Q205 H COPri Gc Q209 H COPri Gc Q222 H COPri Gc Q225 H COPri G.sub.3 Q229 H COPri Gc Q246 H COPri Gc Q201 H COPh Gc Q202 H COPh G.sub.3 Q205 H COPh Gc Q209 H COPh Gc Q222 H COPh G.sub.3 Q225 H COPh Gc Q229 H COPh Gc Q246 H COPh G.sub.3 Q201 H CN Gc CH.sub.2 - Q201 H CN G.sub.3 Q202 H CN Gc Q205 H CN Gc Q209 H CN Gc Q222 H CN Gc Q225 H CN Gc Q229 H CN Gc Q246 H CN G.sub.3 Q201 H H Gc Q202 H H G.sub.3 Q205 H H Gc Q207 H H Gc Q222 H H Gc Q225 H HG.sub.3 Q229 H H Gc Q230 H H Gc Q231 H H G.sub.3 Q237 H H Gc Q246 H H Gc Q247 H H G.sub.3 Q250 H H Gc Q259 H H G.sub.3 Q260 H H Gc Q263 H H G.sub.3 Q201 H Me Gc Q202 H Me G.sub.3 Q205 H Me Gc Q207 H Me G.sub.3 Q222 H Me Gc Q225 H Me Gc Q229 H Me Gc Q230 H Me G.sub.3 Q231 H Me Gc Q237 H Me Gc Q246 H Me Gc Q247 H Me G.sub.3 Q250 H Me Gc Q259 H Me Gc Q260 H Me Gc Q263 H Me G.sub.3 Q201 H Et Gc Q202 H Et G.sub.1 Q205 H Et Gc Q209 H Et Gc Q222 H Et G.sub.3 Q225 H Et Gc Q229H Et Gc Q246 H Et G.sub.2 Q201 H Pri Gc Q205 H Pri Gc Q209 H Pri Gc Q222 H Pri G.sub.3 Q229 H Pri Gc Q201 H CHCH.sub.2 Gc Q205 H CHCH.sub.2 G.sub.3 Q209 H CHCH.sub.2 Gc Q229 H CHCH.sub.2 G.sub.3 Q201 H CHCHMe Gc Q205 H CHCHMe Gc Q201 HCH.sub.2 CHCH.sub.2 Gc Q205 H CH.sub.2 CHCH.sub.2 G.sub.3 Q209 H CH.sub.2 CHCH.sub.2 Gc Q229 H CH.sub.2 CHCH.sub.2 Gc Q201 H CH.sub.2 Cl Gc Q205 H CH.sub.2 Cl G.sub.3 Q209 H CH.sub.2 Cl Gc Q229 H CH.sub.2 Cl Gc Q201 H CH.sub.2 CH.sub.2 Cl Gc Q205 H CH.sub.2 CH.sub.2 Cl G.sub.3 Q209 H CH.sub.2 CH.sub.2 Cl Gc Q229 H CH.sub.2 CH.sub.2 Cl G.sub.2 Q201 H CF.sub.3 Gc Q205 H CF.sub.3 G.sub.3 Q209 H CF.sub.3 Gc Q222 H CF.sub.3 Gc Q225 H CF.sub.3 G.sub.3 Q229 H CF.sub.3 G.sub.1 Q201 HCFCFCl Gc Q205 H CFCFCl Gc Q229 H CFCFCl G.sub.3 Q201 H CH.sub.2 Ph Gc Q205 H CH.sub.2 Ph Gc Q209 H CH.sub.2 Ph G.sub.3 Q201 H Ph Gc Q202 H Ph G.sub.1 Q205 H Ph Gc Q209 H Ph Gc Q222 H Ph G.sub.3 Q225 H Ph Gc Q229 H Ph Gc Q246 H Ph G.sub.2 Q201 H Ph2-Cl Gc Q205 H Ph2-Cl G.sub.1 Q209 H Ph2-Cl Gc Q201 H Ph2-Me Gc Q205 H Ph2-Me G.sub.3 Q209 H Ph2-Me Gc Q225 H Ph2-Me Gc Q229 H Ph2-Me G.sub.3 Q201 H Cl Gc Q205 H Cl Gc Q207 H Cl G.sub.3 Q222 H Cl Gc Q225 H Cl Gc Q229 H Cl G.sub.1 Q231 H Cl Gc Q246 H Cl Gc Q250 H Cl G.sub.3 Q259 H Cl Gc Q260 H Cl Gc Q201 H Br Gc Q205 H Br G.sub.3 Q207 H Br Gc Q229 H Br Gc Q231 H Br G.sub.3 Q250 H Br Gc Q259 H Br Gc Q260 H Br G.sub.3 Q201 H F Gc Q205 H F G.sub.3 Q209 H F Gc Q229 H FGc Q246 H F G.sub.3 Q201 H I Gc Q205 H I Gc Q209 H I Gc Q222 H I Gc Q201 H NO.sub.2 Gc CH.sub.2 - Q201 H NO.sub.2 G.sub.3 Q202 H NO.sub.2 G.sub.3 Q205 H NO.sub.2 Gc Q207 H NO.sub.2 Gc Q222 H NO.sub.2 G.sub.3 Q225 H NO.sub.2 Gc Q229 HNO.sub.2 Gc Q230 H NO.sub.2 G.sub.1 Q231 H NO.sub.2 Gc Q237 H NO.sub.2 Gc Q246 H NO.sub.2 Gc Q247 H NO.sub.2 G.sub.2 Q250 H NO.sub.2 Gc Q259 H NO.sub.2 Gc Q260 H NO.sub.2 G.sub.3 Q263 H NO.sub.2 Gc Q201 H NH.sub.2 Gc Q202 H NH.sub.2 G.sub.3 Q205 H NH.sub.2 Gc Q209 H NH.sub.2 Gc Q222 H NH.sub.2 G.sub.3 Q225 H NH.sub.2 Gc Q229 H NH.sub.2 Gc Q246 H NH.sub.2 G.sub.3 Q201 H NHMe Gc Q205 H NHMe Gc Q209 H NHMe Gc Q225 H NHMe Gc Q229 H NHMe G.sub.3 Q201 H NMe.sub.2 Gc Q205 H NMe.sub.2Gc Q209 H NMe.sub.2 Gc Q222 H NMe.sub.2 G.sub.1 Q225 H NMe.sub.2 Gc Q229 H NMe.sub.2 Gc Q246 H NMe.sub.2 G.sub.3 Q201 H NMeEt Gc Q205 H NMeEt Gc Q209 H NMeEt G.sub.3 Q222 H NMeEt Gc Q225 H NMeEt Gc Q229 H NMeEt G.sub.2 Q201 H NHCOMe Gc Q202H NHCOMe G.sub.3 Q205 H NHCOMe Gc Q209 H NHCOMe Gc Q222 H NHCOMe G.sub.3 Q225 H NHCOMe Gc Q229 H NHCOMe Gc Q246 H NHCOMe G.sub.3 Q201 H NHCOEt Gc Q205 H NHCOEt Gc Q209 H NHCOEt Gc Q222 H NHCOEt G.sub.1 Q225 H NHCOEt Gc Q229 H NHCOEt G.sub.3 Q201 H NHSO.sub.2 Me Gc Q205 H NHSO.sub.2 Me Gc Q209 H NHSO.sub.2 Me Gc Q225 H NHSO.sub.2 Me G.sub.3 Q229 H NHSO.sub.2 Me G.sub.3 Q201 H OMe Gc Q205 H OMe Gc Q209 H OMe G.sub.3 Q222 H OMe Gc Q225 H OMe Gc Q229 H OMe G.sub.2 Q246 H OMe G.sub.1 Q201 H OEt Gc Q205 H OEt Gc Q209 H OEt Gc Q222 H OEt G.sub.3 Q229 H OEt Gc Q201 H CH.sub.2 OMe Gc Q205 H CH.sub.2 OMe Gc Q209 H CH.sub.2 OMe G.sub.3 Q222 H CH.sub.2 OMe Gc Q201 H SMe Gc Q205 H SMe Gc Q209 H SMe Gc Q222 H SMe G.sub.1 Q225 HSMe Gc Q229 H SMe G.sub.3 Q201 H SO.sub.2 Me Gc CH.sub.2 - Q201 H SO.sub.2 Me G.sub.3 Q202 H SO.sub.2 Me Gc Q205 H SO.sub.2 Me Gc Q209 H SO.sub.2 Me Gc Q222 H SO.sub.2 Me G.sub.3 Q225 H SO.sub.2 Me Gc Q229 H SO.sub.2 Me Gc Q246 H SO.sub.2 Me G.sub.3 Q201 HSO.sub.2 Ph Gc Q202 H SO.sub.2 Ph G.sub.1 Q205 H SO.sub.2 Ph Gc Q209 H SO.sub.2 Ph Gc Q222 H SO.sub.2 Ph Gc Q225 H SO.sub.2 Ph G.sub.3 Q229 H SO.sub.2 Ph Gc Q246 H SO.sub.2 Ph G.sub.1 Q201 H SO.sub.2 OMe Gc Q205 H SO.sub.2 OMe Gc Q209 HSO.sub.2 OMe Gc Q222 H SO.sub.2 OMe Gc Q229 H SO.sub.2 OMe G.sub.3 Q201 H SO.sub.2 NH.sub.2 Gc Q205 H SO.sub.2 NH.sub.2 Gc Q209 H SO.sub.2 NH.sub.2 G.sub.3 Q225 H SO.sub.2 NH.sub.2 Gc Q229 H SO.sub.2 NH.sub.2 Gc Q246 H SO.sub.2 NH.sub.2 G.sub.1 Q201 H SO.sub.2 NHMe Gc Q205 H SO.sub.2 NHMe Gc Q209 H SO.sub.2 NHMe G.sub.3 Q222 H SO.sub.2 NHMe Gc Q225 H SO.sub.2 NHMe Gc Q229 H SO.sub.2 NHMe Gc Q246 H SO.sub.2 NHMe G.sub.2 Q201 H SO.sub.2 NMe.sub.2 Gc Q202 H SO.sub.2 NMe.sub.2 G.sub.3 Q205 H SO.sub.2 NMe.sub.2 Gc Q209 H SO.sub.2 NMe.sub.2 Gc Q222 H SO.sub.2 NMe.sub.2 G.sub.2 Q225 H SO.sub.2 NMe.sub.2 Gc Q229 H SO.sub.2 NMe.sub.2 Gc Q246 H SO.sub.2 NMe.sub.2 G.sub.3 Q201 Me COOMe Gc CH.sub.2 - Q201 Me COOMeG.sub.3 Q202 Me COOMe G.sub.1 Q205 Me COOMe Gc Q207 Me COOMe G.sub.3 Q209 Me COOMe Gc Q222 Me COOMe Gc Q225 Me COOMe G.sub.2 Q229 Me COOMe Gc Q230 Me COOMe Gc Q231 Me COOMe G.sub.3 Q237 Me COOMe Gc Q246 Me COOMe Gc Q247 Me COOMe G.sub.3 Q250Me COOMe Gc Q259 Me COOMe G.sub.1 Q260 Me COOMe Gc Q263 Me COOMe G.sub.3 Q201 Me COOEt Gc CH.sub.2 - Q201 Me COOEt G.sub.2 Q222 Me COOEt Gc Q205 Me COOEt Gc Q207 Me COOEt G.sub.3 Q209 Me COOEt Gc Q222 Me COOEt Gc Q225 Me COOEt G.sub.3 Q229Me COOEt Gc Q230 Me COOEt Gc Q231 Me COOEt Gc Q237 Me COOEt G.sub.1 Q246 Me COOEt Gc Q247 Me COOEt Gc Q250 Me COOEt Gc Q259 Me COOEt G.sub.3 Q260 Me COOEt Gc Q263 Me COOEt G.sub.3 Q201 Me COOH G.sub.1 Q205 Me COOH Gc Q201 Me COOPri Gc Q202Me COOPri G.sub.3 Q205 Me COOPri Gc Q209 Me COOPri Gc Q222 Me COOPri G.sub.3 Q225 Me COOPri Gc Q229 Me COOPri Gc Q246 Me COOPri G.sub.1 Q201 Me COOCH.sub.2 CH.sub.2 Cl Gc Q205 Me COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q222 Me COOCH.sub.2 CH.sub.2 Cl Gc Q229 Me COOCH.sub.2 CH.sub.2 Cl G.sub.1 Q201 Me COOCH.sub.2 CHCH.sub.2 Gc Q205 Me COOCH.sub.2 CHCH.sub.2 G.sub.3 Q222 Me COOCH.sub.2 CHCH.sub.2 Gc Q229 Me COOCH.sub.2 CHCH.sub.2 G.sub.1 Q201 Me COOCH.sub.2 CCH Gc Q205 Me COOCH.sub.2 CCH G.sub.2 Q222 Me COOCH.sub.2 CCH Gc Q229 Me COOCH.sub.2 CCH Gc Q201 Me CONHMe Gc Q205 Me CONHMe G.sub.3 Q222 Me CONHMe Gc Q229 Me CONHMe Gc Q201 Me CONMe.sub.2 Gc Q205 Me CONMe.sub.2 G.sub.3 Q222 Me CONMe.sub.2 Gc Q229 Me CONMe.sub.2 Gc Q201Me COMe Gc Q202 Me COMe G.sub.3 Q205 Me COMe Gc Q207 Me COMe Gc Q222 Me COMe G.sub.3 Q225 Me COMe Gc Q229 Me COMe Gc Q230 Me COMe G.sub.3 Q231 Me COMe Gc Q237 Me COMe Gc Q246 Me COMe Gc Q247 Me COMe G.sub.2 Q250 Me COMe Gc Q259 Me COMe Gc Q260 Me COMe G.sub.1 Q263 Me COMe Gc Q201 Me COEt Gc Q205 Me COEt G.sub.3 Q222 Me COEt Gc Q229 Me COEt Gc Q201 Me COPri Gc Q205 Me COPri G.sub.3 Q222 Me COPri Gc Q229 Me COPri G.sub.1 Q201 Me COPh Gc Q205 Me COPh Gc Q222 Me COPh G.sub.3 Q229Me COPh Gc Q201 Me CN Gc Q202 Me CN G.sub.3 Q205 Me CN Gc Q209 Me CN Gc Q222 Me CN G.sub.3 Q225 Me CN Gc Q229 Me CN Gc Q246 Me CN G.sub.1 Q201 Me H Gc Q205 Me H Gc Q222 Me H G.sub.3 Q229 Me H Gc Q201 Me Me Gc Q202 Me Me G.sub.3 Q205 Me MeGc Q209 Me Me Gc Q222 Me Me Gc Q225 Me Me Gc Q229 Me Me G.sub.3 Q246 Me Me Gc Q201 Me Et Gc Q205 Me Et Gc Q222 Me Et G.sub.3 Q229 Me Et Gc Q201 Me Pri Gc Q205 Me Pri G.sub.2 Q201 Me CHCH.sub.2 Gc Q205 Me CHCH.sub.2 G.sub.3 Q201 Me CHCHMeG.sub.3 Q205 Me CHCHMe Gc Q201 Me CH.sub.2 CHCH.sub.2 Gc Q205 Me CH.sub.2 CHCH.sub.2 G.sub.3 Q201 Me CH.sub.2 Cl Gc Q205 Me CH.sub.2 Cl G.sub.2 Q222 Me CH.sub.2 Cl Gc Q229 Me CH.sub.2 Cl G.sub.3 Q201 Me CH.sub.2 CH.sub.2 Cl Gc Q205 MeCH.sub.2 CH.sub.2 Cl Gc Q222 Me CH.sub.2 CH.sub.2 Cl G.sub.3 Q229 Me CH.sub.2 CH.sub.2 Cl Gc Q201 Me CF.sub.3 Gc Q205 Me CF.sub.3 G.sub.3 Q222 Me CF.sub.3 G.sub.3 Q229 Me CF.sub.3 Gc Q201 Me CFCFCl Gc Q205 Me CFCFCl G.sub.3 Q201 Me CH.sub.2Ph Gc Q205 Me CH.sub.2 Ph G.sub.3 Q201 Me Ph Gc Q202 Me Ph Gc Q205 Me Ph Gc Q209 Me Ph Gc Q222 Me Ph G.sub.3 Q225 Me Ph G.sub.3 Q229 Me Ph Gc Q246 Me Ph G.sub.3 Q201 Me Ph2-Cl Gc Q205 Me Ph2-Cl G.sub.3 Q201 Me Ph2-Me Gc Q205 Me Ph2-Me Gc Q229 Me Ph2-Me G.sub.3 Q201 Me Cl Gc Q202 Me Cl G.sub.3 Q205 Me Cl Gc Q209 Me Cl Gc Q222 Me Cl G.sub.3 Q225 Me Cl Gc Q229 Me Cl Gc Q246 Me Cl G.sub.3 Q201 Me Br Gc Q205 Me Br G.sub.3 Q222 Me Br Gc Q229 Me Br G.sub.1 Q201 Me F G.sub.1 Q205Me F G.sub.1 Q201 Me I G.sub.1 Q205 Me I G.sub.1 Q201 Me NO.sub.2 Gc Q202 Me NO.sub.2 G.sub.3 Q205 Me NO.sub.2 Gc Q209 Me NO.sub.2 Gc Q222 Me NO.sub.2 Gc Q225 Me NO.sub.2 G.sub.3 Q229 Me NO.sub.2 Gc Q246 Me NO.sub.2 Gc Q201 Me NH.sub.2 Gc Q205 Me NH.sub.2 G.sub.3 Q222 Me NH.sub.2 Gc Q229 Me NH.sub.2 G.sub. 3 Q201 Me NHMe Gc Q205 Me NHMe Gc Q229 Me NHMe G.sub.3 Q201 Me NMe.sub.2 Gc Q205 Me NMe.sub.2 Gc Q229 Me NMe.sub.2 G.sub.3 Q201 Me NMeEt Gc Q205 Me NMeEt Gc Q201 Me NHCOMe Gc Q205 Me NHCOMe Gc Q222 Me NHCOMe G.sub.3 Q229 Me NHCOMe Gc Q201 Me NHCOEt Gc Q205 MeNHCOEt G.sub.3 Q201 Me NHSO.sub.2 Me Gc Q205 Me NHSO.sub.2 Me Gc Q229 Me NHSO.sub.2 Me G.sub.2 Q201 Me OMe Gc Q205 Me OMe G.sub.3 Q222 Me OMe Gc Q229 Me OMe G.sub.1 Q201 Me OEt Gc Q205 Me OEt G.sub.3 Q201 Me CH.sub.2 OMe Gc Q205 Me CH.sub.2OMe Gc Q229 Me CH.sub.2 OMe G.sub.3 Q201 Me SMe Gc Q205 Me SMe G.sub.3 Q201 Me SO.sub.2 Me Gc Q205 Me SO.sub.2 Me Gc Q222 Me SO.sub.2 Me G.sub.1 Q229 Me SO.sub.2 Me G.sub.3 Q201 Me SO.sub.2 Ph Gc Q205 Me SO.sub.2 Ph Gc Q222 Me SO.sub.2 PhG.sub.3 Q229 Me SO.sub.2 Ph Gc Q201 Me SO.sub.2 OMe Gc Q205 Me SO.sub.2 OMe G.sub.3 Q229 Me SO.sub.2 OMe Gc Q201 Me SO.sub.2 NH.sub.2 Gc Q205 Me SO.sub.2 NH.sub.2 Gc Q229 Me SO.sub.2 NH.sub.2 G.sub.3 Q201 Me SO.sub.2 NHMe Gc Q205 Me SO.sub.2NHMe Gc Q222 Me SO.sub.2 NHMe G.sub.1 Q229 Me SO.sub.2 NHMe Gc Q201 Me SO.sub.2 NMe.sub.2 Gc Q205 Me SO.sub.2 NMe.sub.2 G.sub.3 Q222 Me SO.sub.2 NMe.sub.2 Gc Q229 Me SO.sub.2 NMe.sub.2 G.sub.1 Q201 Et COOMe Gc Q205 Et COOMe Gc Q229 Et COOMeG.sub.3 Q246 Et COOMe G.sub.3 Q201 Et COOEt Gc Q202 Et COOEt G.sub.2 Q209 Et COOEt Gc Q222 Et COOEt G.sub.3 Q225 Et COOEt Gc Q201 Et COOPri G.sub.3 Q205 Et COOPri Gc Q201 Et COOCH.sub.2 CHCl Gc Q205 Et COOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 EtCOOCH.sub.2 CCH Gc Q201 Et CONHMe Gc Q201 Et CONMe.sub.2 Gc Q201 Et COMe Gc Q205 Et COMe G.sub.3 Q229 Et COMe Gc Q201 Et COEt Gc Q201 Et COPh Gc Q201 Et CN Gc Q205 Et CN G.sub.3 Q229 Et CN Gc Q201 Et H Gc Q205 Et H G.sub.3 Q201 Et Me Gc Q205 Et Me G.sub.3 Q201 Et Et Gc Q205 Et Pri Gc Q201 Et CHCHMe Gc Q201 Et CH.sub.2 CH.sub.2 Cl Gc Q201 Et CH.sub.2 Ph G.sub.3 Q201 Et Ph Gc Q205 Et Ph Gc Q209 Et Ph Gc Q229 Et Ph G.sub.3 Q201 Et Ph2-Cl Gc Q205 Et Ph2-Me Gc Q201 Et Cl Gc Q205 Et Cl G.sub.2 Q201 Et Br Gc Q205 Et Br G.sub.1 Q201 Et FGc Q201 Et NO.sub.2 Gc Q205 Et NO.sub.2 G.sub.3 Q209 Et NO.sub.2 Gc Q201 Et NH.sub.2 Gc Q201 Et NHMe Gc Q201 Et NMe.sub.2 Gc Q205 Et NMe.sub.2 G.sub.3 Q201 Et NHCOMe Gc Q205 Et NHCOMe Gc Q201 Et NHCOEt Gc Q201 Et NHSO.sub.2 Me Gc Q201 Et OMeGc Q205 Et OEt G.sub.3 Q201 Et CH.sub.2 OMe Gc Q201 Et SMe Gc Q201 Et SO.sub.2 Me Gc Q205 Et SO.sub.2 Me G.sub.3 Q201 Et SO.sub.2 Ph Gc Q205 Et SO.sub.2 Ph G.sub.3 Q201 Et SO.sub.2 OMe Gc Q201 Et SO.sub.2 NH.sub.2 Gc Q205 Et SO.sub.2 NHMeG.sub.3 Q201 Et SO.sub.2 NMe.sub.2 Gc Q205 Et SO.sub.2 NMe.sub.2 G.sub.3 Q201 Cl COOMe Gc Q209 Cl COOMe G.sub.3 Q229 Cl COOMe Gc Q246 Cl COOMe G.sub.3 Q201 Cl COOEt Gc Q205 Cl COOEt Gc Q222 Cl COOEt G.sub.1 Q225 Cl COOEt Gc Q246 Cl COOEtG.sub.3 Q201 Cl COOPri Gc Q205 Cl COOPri G.sub.3 Q205 Cl COOCH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Cl COOCH.sub.2 CHCH.sub.2 Gc Q201 Cl COOCH.sub.2 CCH G.sub.3 Q201 Cl CONHMe Gc Q201 Cl CONMe.sub.2 G.sub.3 Q201 Cl COMe Gc Q205 Cl COMe Gc Q201 ClCOEt G.sub.3 Q201 Cl COPri Gc Q201 Cl COPh G.sub.3 Q201 Cl CN Gc Q205 Cl CN Gc Q201 Cl H G.sub.3 Q201 Cl Me Gc Q205 Cl Me G.sub.3 Q205 Cl Et Gc Q201 Cl Pri G.sub.3 Q201 Cl CHCHMe Gc Q201 Cl CH.sub.2 CH CH.sub.2 G.sub.1 Q205 Cl CH.sub.2CH.sub.2 Cl Gc Q201 Cl Ph Gc Q205 Cl Ph Gc Q209 Cl Ph G.sub.3 Q201 Cl Ph2-Cl Gc Q205 Cl Ph2-Me G.sub.3 Q201 Cl Cl Gc Q205 Cl Cl G.sub.3 Q201 Cl Br Gc Q201 Cl NO.sub.2 Gc Q205 Cl NO.sub.2 G.sub.3 Q209 Cl NO.sub.2 Gc Q201 Cl NH.sub.2 Gc Q201Cl NHMe G.sub.1 Q201 Cl NMe.sub.2 G.sub.3 Q201 Cl NHCOMe Gc Q205 Cl NHCOEt Gc Q201 Cl NHSO.sub.2 Me G.sub.3 Q201 Cl OMe Gc Q201 Cl CH.sub.2 OMe G.sub.3 Q201 Cl SO.sub.2 Me Gc Q201 Cl SO.sub.2 Ph Gc Q201 Cl SO.sub.2 NH.sub.2 G.sub.3 Q201 ClSO.sub.2 NMe.sub.2 Gc Q205 Cl SO.sub.2 NMe.sub.2 Gc Q201 Br COOMe Gc Q205 Br COOMe G.sub.3 Q209 Br COOMe G.sub.3 Q201 Br COOEt Gc Q209 Br COOEt Gc Q229 Br COOEt G.sub.3 Q201 Br COOPri G.sub.3 Q201 Br COOCH.sub.2 CH.sub.2 Cl Gc Q201 BrCOOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 Br CONHMe Gc Q201 Br CONMe.sub.2 G.sub. 3 Q201 Br COMe Gc Q205 Br COMe G.sub.3 Q201 Br COEt Gc Q201 Br COPh G.sub.3 Q201 Br CN Gc Q205 Br CN Gc Q201 Br H G.sub.3 Q201 Br Me G.sub.2 Q201 Br Et G.sub.1 Q201Br CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Br Ph Gc Q205 Br Ph Gc Q209 Br Ph G.sub.3 Q201 Br Ph2-Cl G.sub.3 Q201 Br Cl Gc Q201 Br Br Gc Q205 Br Br G.sub.3 Q201 Br NO.sub.2 Gc Q209 Br NO.sub.2 Gc Q201 Br NH.sub.2 Gc Q201 Br NMe.sub.2 G.sub.3 Q201Br NHCOMe Gc Q201 Br OMe G.sub.3 Q201 Br CH.sub.2 OMe Gc Q201 Br SMe Gc Q201 Br SO.sub.2 Me Gc Q201 Br SO.sub.2 NH.sub.2 G.sub.3 Q201 Br SO.sub.2 NHMe Gc Q201 Br SO.sub.2 NMe.sub.2 G.sub.3 Q201 SMe COOMe Gc Q205 SMe COOMe Gc Q209 SMe COOMeG.sub.3 Q201 SMe COOEt Gc Q205 SMe COOEt Gc Q209 SMe COOEt Gc Q229 SMe COOEt G.sub.3 Q246 SMe COOEt Gc Q201 SMe COOPri Gc Q205 SMe COOPri G.sub.3 Q201 SMe COOCH.sub.2 CH.sub.2 Cl Gc Q201 SMe COOCH.sub.2 CHCH.sub.2 Gc Q201 SMe CONHMe Gc Q201SMe CONMe.sub.2 G.sub.1 Q201 SMe COMe Gc Q205 SMe COMe Gc Q201 SMe COEt G.sub.3 Q201 SMe COPri Gc Q201 SMe COPh G.sub.3 Q201 SMe CN Gc Q205 SMe CN Gc Q229 SMe CN G.sub.3 Q201 SMe H Gc Q201 SMe Me Gc Q205 SMe Me G.sub.3 Q201 SMe Et Gc Q205SMe Et Gc Q201 SMe CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 SMe Ph Gc Q205 SMe Ph Gc Q209 SMe Ph G.sub.3 Q201 SMe Ph2-Cl Gc Q201 SMe Cl Gc Q205 SMe Cl G.sub.3 Q201 SMe Br Gc Q201 SMe NO.sub.2 Gc Q205 SMe NO.sub.2 Gc Q209 SMe NO.sub.2 G.sub.3 Q201SMe NH.sub.2 Gc Q205 SMe NH.sub.2 Gc Q201 SMe NHMe G.sub.3 Q201 SMe NMe.sub.2 Gc Q205 SMe NMe.sub.2 Gc Q201 SMe NHCOMe Gc Q205 SMe NHCOMe G.sub.3 Q201 SMe NHSO.sub.2 Me Gc Q201 SMe OMe Gc Q201 SMe CH.sub.2 OMe Gc Q201 SMe SMe Gc Q201 SMeSO.sub.2 Me Gc Q205 SMe SO.sub.2 Me G.sub.3 Q201 SMe SO.sub.2 Ph Gc Q201 SMe SO.sub.2 NH.sub.2 Gc Q201 SMe SO.sub.2 NHMe G.sub.3 Q201 SMe SO.sub.2 NMe.sub.2 Gc Q201 SO.sub.2 Me COOMe Gc Q205 SO.sub.2 Me COOMe Gc Q209 SO.sub.2 Me COOMeG.sub.3 Q229 SO.sub.2 Me COOMe G.sub.3 Q246 SO.sub.2 Me COOMe G.sub.1 Q201 SO.sub.2 Me COOEt Gc Q205 SO.sub.2 Me COOEt Gc Q209 SO.sub.2 Me COOEt G.sub.3 Q222 SO.sub.2 Me COOEt Gc Q225 SO.sub.2 Me COOEt Gc Q201 SO.sub.2 Me COOPri G.sub.3 Q205 SO.sub.2 Me COOPri Gc Q201 SO.sub.2 Me COOCH.sub.2 CH.sub.2 Cl Gc Q201 SO.sub.2 Me COOCH.sub.2 CHCH.sub.2 G.sub.3 Q201 SO.sub.2 Me COOCH.sub.2 CCH Gc Q201 SO.sub.2 Me CONHMe Gc Q201 SO.sub.2 Me CONMe.sub.2 G.sub.2 Q201 SO.sub.2 Me COMe Gc Q205 SO.sub.2 Me COMe Gc Q229 SO.sub.2 Me COMe G.sub.3 Q201 SO.sub.2 Me COEt Gc Q205 SO.sub.2 Me COEt Gc Q201 SO.sub.2 Me COPri G.sub.3 Q201 SO.sub.2 Me COPh Gc Q201 SO.sub.2 Me CN Gc Q205 SO.sub.2 Me CN Gc Q222 SO.sub.2 Me CN Gc Q229 SO.sub.2 Me CN Gc Q201 SO.sub.2 Me H G.sub.2 Q201 SO.sub.2 Me Me Gc Q205 SO.sub.2 Me Me Gc Q201 SO.sub.2 Me Et G.sub.3 Q201 SO.sub.2 Me Pri Gc Q201 SO.sub.2 Me CHCH.sub.2 Gc Q201 SO.sub.2 Me CHCHMe G.sub.1 Q201 SO.sub.2 Me CH.sub.2 CH.sub.2 Cl Gc Q205 SO.sub.2 Me CH.sub.2CH.sub.2 Cl G.sub.3 Q201 SO.sub.2 Me CH.sub.2 Ph G.sub.3 Q201 SO.sub.2 Me Ph Gc Q205 SO.sub.2 Me Ph Gc Q209 SO.sub.2 Me Ph Gc Q229 SO.sub.2 Me Ph G.sub.3 Q246 SO.sub.2 Me Ph G.sub.3 Q201 SO.sub.2 Me Ph2-Cl Gc Q205 SO.sub.2 Me Ph2-Me Gc Q201 SO.sub.2 Me Cl Gc Q205 SO.sub.2 Me Cl Gc Q229 SO.sub.2 Me Cl G.sub.3 Q201 SO.sub.2 Me Br G.sub.3 Q205 SO.sub.2 Me Br Gc Q201 SO.sub.2 Me NO.sub.2 Gc Q205 SO.sub.2 Me NO.sub.2 Gc Q209 SO.sub.2 Me NO.sub.2 Gc Q229 SO.sub.2 Me NO.sub.2G.sub.3 Q201 SO.sub.2 Me NH.sub.2 Gc Q205 SO.sub.2 Me NH.sub.2 G.sub.3 Q201 SO.sub.2 Me NHMe Gc Q201 SO.sub.2 Me NMe.sub.2 Gc Q205 SO.sub.2 Me NMe.sub.2 G.sub.1 Q201 SO.sub.2 Me NHCOMe Gc Q205 SO.sub.2 Me NHCOMe Gc Q201 SO.sub.2 Me NHCOEtG.sub.3 Q201 SO.sub.2 Me NHSO.sub.2 Me Gc Q201 SO.sub.2 Me OMe G.sub.1 Q201 SO.sub.2 Me CH.sub.2 OMe Gc Q205 SO.sub.2 Me CH.sub.2 OMe Gc Q201 SO.sub.2 Me SO.sub.2 Me Gc Q205 SO.sub.2 Me SO.sub.2 Me Gc Q201 SO.sub.2 Me SO.sub.2 Ph G.sub.3 Q201 SO.sub.2 Me SO.sub.2 OMe Gc Q201 SO.sub.2 Me SO.sub.2 NH.sub.2 Gc Q201 SO.sub.2 Me SO.sub.2 NHMe G.sub.3 Q201 SO.sub.2 Me SO.sub.2 NMe.sub.2 Gc Q201 Ph COOMe Gc Q205 Ph COOMe G.sub.3 Q209 Ph COOMe Gc Q201 Ph COOEt Gc Q205 Ph COOEt Gc Q209 Ph COOEt G.sub.3 Q229 Ph COOEt Gc Q201 Ph COOPri G.sub.3 Q201 Ph COOCH.sub.2 CH.sub.2 Cl Gc Q201 Ph COOCH.sub.2 CHCH.sub.2 Gc Q201 Ph COOCH.sub.2 CCH G.sub.3 Q201 Ph CONMe.sub.2 Gc Q201 Ph COMe Gc Q205 Ph COMe Gc Q201 Ph COEt G.sub.3 Q201 Ph CN Gc Q205 Ph CN Gc Q201 Ph H G.sub.3 Q201 Ph Me Gc Q201 Ph Et Gc Q201 Ph CH.sub.2 CH.sub.2 Cl G.sub.3 Q201 Ph Ph Gc Q205 Ph Ph Gc Q209 Ph Ph G.sub.3 Q201 Ph Cl Gc Q201 Ph Br G.sub.3 Q201 Ph NO.sub.2 Gc Q201 Ph NH.sub.2 Gc Q201 PhNHMe G.sub.3 Q201 Ph NMe.sub.2 Gc Q201 Ph NHCOMe Gc Q201 Ph NHSO.sub.2 Me G.sub.1 Q201 Ph CH.sub.2 OMe Gc Q201 Ph SO.sub.2 Me G.sub.3 Q201 Ph SO.sub.2 NH.sub.2 Gc Q201 Ph SO.sub.2 NHMe Gc Q201 Ph SO.sub.2 NMe.sub.2 G.sub.3 ______________________________________ TABLE 4 ______________________________________ ##STR26## A B D E W Gn ______________________________________ Q5 H H Me O Gc CH.sub.2Q5 H H Me O Gc Q5 H H Et O G3 Q5 H H Prn O G3 Q5 H H CH.sub.2 CHCH.sub.2 O G3 Q5 H H OMe O G3 Q61 H HMe O Gc CH.sub.2Q61 H H Me O Gc Q61 H H Et O G3 Q61 H H Prn O G3 Q61 H H CH.sub.2 CHCH.sub.2 O G3 Q61 H H OMe O G3 Q26 H H Me O G3 Q26 H H Et O G3 Q26 H H OMe O G3 Q5 H H H S Gc CH.sub.2Q5 H H H S G3 Q26 H H H S Gc Q61 H H H S Gc CH.sub.2Q61 H H H S G3 Q5 H H H NH Gc CH.sub.2Q5 H H H NH G3 Q26 H H H NH Gc Q61 H H H NH Gc CH.sub.2Q61 H H H NH G3 Q5 H H H NOMe Gc CH.sub.2Q5 H H H NOMe G3 Q26 H H H NOMe Gc Q61 H H H NOMe Gc CH.sub.2Q61 H H H NOMe G3 Q201 H H Me O Gc CH.sub.2Q201 H H Me O G.sub.3 Q201 H H Et O Gc Q201 H H Prn O G.sub.3 Q201 H H CH.sub.2 CHCH.sub.2 O Gc Q201 H H OMe O Gc Q205 H H Me O G.sub.3 Q205 H H Et O G.sub.3 Q205 H H OMe O G.sub.3 Q201 H H H S Gb CH.sub.2Q201 H H H S G.sub.3 Q205 HH H S Gc Q222 H H H S G.sub.2 Q229 H H H S G.sub.3 Q201 H H H NH Gb CH.sub.2Q201 H H H NH G.sub.3 Q205 H H H NH Gc Q222 H H H NH G.sub.3 Q229 H H H NH G.sub.3 Q201 H H H NOMe Gb CH.sub.2Q201 H H H NOMe G.sub.3 Q205 H H H NOMe Gc Q222 H H HNOMe Gc Q229 H H H NOMe G.sub.3 ______________________________________ TABLE 5 ______________________________________ ##STR27## A B D W2 R22 Gn ______________________________________ Q5 H H O Me Gc CH.sub.2Q5 H H O Me G3 Q5 H H O Et Gc Q5 H H O Prn G3 Q26 H H O Me Gc Q26 H H O Et G3 Q61 H H O Me Gc CH.sub.2Q61 H H O Me Gc Q61 H H O Et Gc Q61 H H O Prn G3 Q158 H H O Et G3 Q158 H H O Me G3 Q5 H H S Me Gc CH.sub.2Q5 H H S Me G3 Q5 H H S Et Gc Q5 H H S Prn G3 Q26 H H S Me Gc Q26 H H S Et G3 Q61 H H S Me Gc CH.sub.2Q61 H H S Me Gc Q61 H H SEt Gc Q61 H H S Prn G3 Q158 H H S Et G3 Q158 H H S Me G3 Q201 H H O Me Gc CH.sub.2Q201 H H O Me G.sub.3 Q201 H H O Et Gc Q201 H H O Prn Gc Q205 H H O Me G.sub.3 Q205 H H O Et Gc Q222 H H O Me Gc Q222 H H O Et G.sub.3 Q229 H H O Me Gc Q229 HH O Et G.sub.3 Q201 H H S Me Gc CH.sub.2Q201 H H S Me G.sub.3 Q201 H H S Et Gc Q201 H H S Prn Gc Q205 H H S Me Gc Q205 H H S Et Gc Q222 H H S Me G.sub.3 Q222 H H S Et Gc Q229 H H S Me Gc Q229 H H S Et G.sub.3 ______________________________________ TABLE 6 ______________________________________ ##STR28## A B D Az Gn ______________________________________ Q5 H H Imidazol-1-yl Gc Q5 H H Pyrazol-1-yl Gc CH.sub.2Q5 H H Imidazol-1-yl G3 CH.sub.2Q5 H H Pyrazol-1-yl G3 Q26 H HImidazol-1-yl Gc Q26 H H Pyrazol-1-yl Gc Q61 H H Imidazol-1-yl Gc Q61 H H Pyrazol-1-yl Gc CH.sub.2Q61 H H Imidazol-1-yl G3 CH.sub.2Q61 H H Pyrazol-1-yl G3 Q158 H H Imidazol-1-yl G3 Q158 H H Pyrazol-1-yl G3 Q201 H H Imidazol-1-yl Gc Q201H H Pyrazol-1-yl Gc CH.sub.2Q201 H H Imidazol-1-yl G.sub.3 CH.sub.2Q201 H H Pyrazol-1-yl G.sub.3 Q205 H H Imidazol-1-yl Gc Q205 H H Pyrazol-1-yl Gc Q222 H H Imidazol-1-yl G.sub.3 Q222 H H Pyrazol-1-yl G.sub.3 Q229 H H Imidazol-1-yl Gc Q229 H H Pyrazol-1-yl Gc ______________________________________ TABLE 7 ______________________________________ ##STR29## A B D J R23 Gn ______________________________________ Q5 H H Me H Gc Q5 H H Me Me G3 Q5 H H Me OMe Gc Q5 H H Et H G3 Q5 H H Et Me G3 Q5 H H Et OMe Gc Q5 H H J1 H G3 Q5 H H J1 MeG1 Q5 H H J1 OMe G3 Q201 H H Me H Gc Q201 H H Me Me G.sub.3 Q201 H H Me OMe Gc Q201 H H Et H G.sub.3 Q201 H H Et Me G.sub.3 Q201 H H Et OMe Gc Q201 H H J10 H G.sub.3 Q201 H H J10 Me G.sub.1 Q201 H H J10 OMe G.sub.3 ______________________________________ TABLE 8 ______________________________________ ##STR30## A B D E W Gn ______________________________________ Q5 H COOMe Me O Gc CH.sub.2Q5 H COOMe Me O G3 Q5 H COOMe Et O Gc Q5 H COOMe Prn O Gc Q5 H COOMe CH.sub.2 CHCH.sub.2 O G3 Q5 HCOOMe OMe O Gc Q26 H COOMe Me O G3 Q26 H COOMe Et O Gc Q26 H COOMe OMe O Gc Q61 H COOMe Me O Gc CH.sub.2Q61 H COOMe Me O G3 Q61 H COOMe Et O Gc Q61 H COOMe Prn O Gc Q61 H COOMe CH.sub.2 CHCH.sub.2 O G3 Q61 H COOMe OMe O Gc Q5 H COOMe H S Gb CH.sub.2Q5 H COOMe H S G3 Q26 H COOMe H S Gc Q61 H COOMe H S Gc CH.sub.2Q61 H COOMe H S G3 Q5 H COOMe H NH Gb CH.sub.2Q5 H COOMe H NH G3 Q26 H COOMe H NH Gc Q61 H COOMe H NH Gc CH.sub.2Q61 H COOMe H NH G3 Q5 H COOMe H NOMe Gb CH.sub.2Q5 HCOOMe H NOMe G3 Q26 H COOMe H NOMe Gc Q61 H COOMe H NOMe Gc CH.sub.2Q61 H COOMe H NOMe G3 Q5 H COOEt Me O Gc CH.sub.2Q5 H COOEt Me O G3 Q5 H COOEt Et O Gc Q5 H COOEt Prn O Gc Q5 H COOEt CH.sub.2 CHCH.sub.2 O G3 Q5 H COOEt OMe O Gc Q26 HCOOEt Me O G3 Q26 H COOEt Et O Gc Q26 H COOEt OMe O Gc Q61 H COOEt Me O Gc CH.sub.2Q61 H COOEt Me O G3 Q61 H COOEt Et O Gc Q61 H COOEt Prn O Gc Q61 H COOEt CH.sub.2 CHCH.sub.2 O G3 Q61 H COOEt OMe O Gc Q5 H COOEt H S Gb CH.sub.2Q5 H COOEt HS G3 Q26 H COOEt H S Gc Q61 H COOEt H S Gc CH.sub.2Q61 H COOEt H S G3 Q5 H COOEt H NH Gb CH.sub.2Q5 H COOEt H NH G3 Q26 H COOEt H NH Gc Q61 H COOEt H NH Gc CH.sub.2Q61 H COOEt H NH G3 Q5 H COOEt H NOMe Gb CH.sub.2Q5 H COOEt H NOMe G3 Q26 HCOOEt H NOMe Gc Q61 H COOEt H NOMe Gc CH.sub.2Q61 H COOEt H NOMe G3 Q201 H COOMe Me O Gc CH.sub.2Q201 H COOMe Me O G.sub.3 Q201 H COOMe Et O Gc Q201 H COOMe Prn O Gc Q201 H COOMe CH.sub.2 CHCH.sub.2 O G.sub.3 Q201 H COOMe OMe O Gc Q205 HCOOMe Me O G.sub.3 Q205 H COOMe Et O Gc Q205 H COOMe OMe O Gc Q201 H COOMe H S Gb CH.sub.2Q201 H COOMe H S G.sub.3 Q205 H COOMe H S Gc Q222 H COOMe H S G.sub.3 Q229 H COOMe H S G.sub.1 Q201 H COOMe H NH Gb CH.sub.2Q201 H COOMe H NH G.sub.3 Q205 H COOMe H NH Gc Q222 H COOMe H NH Gc Q229 H COOMe H NH G.sub.3 Q201 H COOMe H NOMe Gb CH.sub.2Q201 H COOMe H NOMe G.sub.3 Q205 H COOMe H NOMe Gc Q222 H COOMe H NOMe Gc Q229 H COOMe H NOMe G.sub.3 Q201 H COOEt Me O Gc CH.sub.2Q201 H COOEtMe O G.sub.3 Q201 H COOEt Et O Gc Q201 H COOEt Prn O Gc Q201 H COOEt CH.sub.2 CHCH.sub.2 O Gc Q201 H COOEt OMe O Gc Q205 H COOEt Me O G.sub.3 Q205 H COOEt Et O G.sub.3 Q205 H COOEt OMe O Gc Q201 H COOEt H S Gb CH.sub.2Q201 H COOEt H S G.sub.3 Q205 H COOEt H S Gc Q222 H COOEt H S Gc Q229 H COOEt H S Gc Q201 H COOEt H NH Gb CH.sub.2Q201 H COOEt H NH G.sub.3 Q205 H COOEt H NH Gc Q222 H COOEt H NH Gc Q229 H COOEt H NH Gc Q201 H COOEt H NOMe Gb CH.sub.2Q201 H COOEt H NOMe G.sub.3 Q205H COOEt H NOMe Gc Q222 H COOEt H NOMe Gc Q229 H COOEt H NOMe G.sub. 3 ______________________________________ TABLE 9 ______________________________________ ##STR31## A B D W2 R22 Gn ______________________________________ Q5 H COOMe O Me Gc CH.sub.2Q5 H COOMe O Me G3 Q5 H COOMe O Et Gc Q5 H COOMe O Prn G3 Q26 H COOMe O Me Gc Q26 H COOMe O Et G3 Q61 H COOMe O Me Gc CH.sub.2Q61 H COOMe O Me G3 Q61 H COOMe O Et Gc Q61 H COOMe O Prn G3 Q158 H COOMe O Me Gc Q158 H COOMe O Et G3 Q5 H COOMe S Me Gc CH.sub.2Q5 H COOMe S Me G3 Q5 H COOMe S Et Gc Q5 H COOMe S Prn G3 Q26 H COOMe S Me Gc Q26 HCOOMe S Et G3 Q61 H COOMe S Me Gc CH.sub.2Q61 H COOMe S Me G3 Q61 H COOMe S Et Gc Q61 H COOMe S Prn G3 Q158 H COOMe S Me Gc Q158 H COOMe S Et G3 Q5 H COOEt O Me Gc CH.sub.2Q5 H COOEt O Me G3 Q5 H COOEt O Et Gc Q5 H COOEt O Prn G3 Q26 H COOEtO Me Gc Q26 H COOEt O Et G3 Q61 H COOEt O Me Gc CH.sub.2Q61 H COOEt O Me G3 Q61 H COOEt O Et Gc Q61 H COOEt O Prn G3 Q158 H COOEt O Me Gc Q158 H COOEt O Et G3 Q5 H COOEt S Me Gc CH.sub.2Q5 H COOEt S Me G3 Q5 H COOEt S Et Gc Q5 H COOEt S PrnG3 Q26 H COOEt S Me Gc Q26 H COOEt S Et G3 Q61 H COOEt S Me Gc CH.sub.2Q61 H COOEt S Me G3 Q61 H COOEt S Et Gc Q61 H COOEt S Prn G3 Q158 H COOEt S Me Gc Q158 H COOEt S Et G3 Q201 H COOMe O Me Gc CH.sub.2Q201 H COOMe O Me G3 Q201 H COOMe O EtGc Q201 H COOMe O Prn Gc Q205 H COOMe O Me Gc Q205 H COOMe O Et Gc Q222 H COOMe O Me Gc Q222 H COOMe O Et G3 Q229 H COOMe O Me G3 Q229 H COOMe O Et Gc Q201 H COOMe S Me Gc CH.sub.2Q201 H COOMe S Me G3 Q201 H COOMe S Et Gc Q201 H COOMe S PrnGc Q205 H COOMe S Me Gc Q205 H COOMe S Et Gc Q222 H COOMe S Me Gc Q222 H COOMe S Et G3 Q229 H COOMe S Me Gc Q229 H COOMe S Et G3 Q201 H COOEt O Me Gc CH.sub.2Q201 H COOEt O Me G3 Q201 H COOEt O Et Gc Q201 H COOEt O Prn Gc Q205 H COOEt O Me Gc Q205 H COOEt O Et Gc Q222 H COOEt O Me Gc Q222 H COOEt O Et G3 Q229 H COOEt O Me Gc Q229 H COOEt O Et G3 Q201 H COOEt S Me Gc CH.sub.2Q201 H COOEt S Me G3 Q201 H COOEt S Et Gc Q201 H COOEt S Prn Gc Q205 H COOEt S Me Gc Q205 H COOEt S Et G3 Q222 H COOEt S Me Gc Q222 H COOEt S Et Gc Q229 H COOEt S Me G1 Q229 H COOEt S Et G1 ______________________________________ TABLE 10 ______________________________________ ##STR32## A B D Az Gn ______________________________________ Q5 H COOMe Imidazol-1-yl Gc Q5 H COOMe Pyrazol-1-yl Gc CH.sub.2Q5 H COOMe Imidazol-1-yl G1 CH.sub.2Q5 H COOMe Pyrazol-1-yl G1 Q26 H COOMe Imidazol-1-yl Gc Q26 H COOMe Pyrazol-1-yl Gc Q61 H COOMe Imidazol-1-yl Gc Q61 H COOMe Pyrazol-1-yl Gc CH.sub.2Q61 H COOMe Imidazol-1-yl G3 CH.sub.2Q61 H COOMe Pyrazol-1-yl G3 Q5 H COOEt Imidazol-1-yl Gc Q5 H COOEt Pyrazol-1-yl Gc CH.sub.2Q5 H COOEt Imidazol-1-yl G3 CH.sub.2Q5 H COOEt Pyrazol-1-yl G3 Q26 H COOEt Imidazol-1-yl Gc Q26 H COOEt Pyrazol-1-yl Gc Q61 H COOEt Imidazol-1-yl Gc Q61 H COOEt Pyrazol-1-yl Gc CH.sub.2Q61 H COOEt Imidazol-1-yl G3 CH.sub.2Q61 HCOOEt Pyrazol-1-yl G3 Q201 H COOMe Imidazol-1-yl Gc Q201 H COOMe Pyrazol-1-yl Gc CH.sub.2Q201 H COOMe Imidazol-1-yl G1 CH.sub.2Q201 H COOMe Pyrazol-1-yl G1 Q205 H COOMe Imidazol-1-yl Gc Q205 H COOMe Pyrazol-1-yl Gc Q222 H COOMeImidazol-1-yl Gc Q222 H COOMe Pyrazol-1-yl Gc Q229 H COOMe Imidazol-1-yl G3 Q229 H COOMe Pyrazol-1-yl G3 Q201 H COOEt Imidazol-1-yl Gc Q201 H COOEt Pyrazol-1-yl Gc CH.sub.2Q201 H COOEt Imidazol-1-yl G3 CH.sub.2Q201 H COOEt Pyrazol-1-yl G3 Q205 H COOEt Imidazol-1-yl Gc Q205 H COOEt Pyrazol-1-yl Gc Q222 H COOEt Imidazol-1-yl Gc Q222 H COOEt Pyrazol-1-yl Gc Q229 H COOEt Imidazol-1-yl G3 Q229 H COOEt Pyrazol-1-yl G3 ______________________________________ TABLE 11 ______________________________________ ##STR33## A B D J R23 Gn ______________________________________ Q5 H COOMe Me H G3 Q5 H COOMe Me Me Gc Q5 H COOMe Me OMe Gc Q5 H COOMe Et H Gc Q5 H COOMe Et Me Gc Q5 H COOMe Et OMe G3 Q5 HCOOMe J2 H Gc Q5 H COOMe J2 Me Gc Q5 H COOMe J2 OMe G3 Q5 H COOEt Me H Gc Q5 H COOEt Me Me G3 Q5 H COOEt Me OMe Gc Q5 H COOEt Et H Gc Q5 H COOEt Et Me G3 Q5 H COOEt Et OMe Gc Q5 H COOEt J3 H Gc Q5 H COOEt J3 Me Gc Q5 H COOEt J3 OMe Gc CH.sub.2Q5 H COOMe Me H G3 CH.sub.2Q5 H COOEt Me OMe Gc Q26 H COOMe Me H Gc Q26 H COOEt Me OMe Gc Q61 H COOMe Me H G3 Q61 H COOMe Me Me Gc Q61 H COOMe Me OMe Gc Q61 H COOMe Et H Gc Q61 H COOMe Et Me Gc Q61 H COOMe Et OMe G3 Q61 H COOMe J4 H Gc Q61 H COOMe J4 Me Gc Q61 H COOMe J4 OMe G3 Q61 H COOEt Me H Gc Q61 H COOEt Me Me G3 Q61 H COOEt Me OMe Gc Q61 H COOEt Et H Gc Q61 H COOEt Et Me G3 Q61 H COOEt Et OMe Gc Q61 H COOEt J5 H Gc Q61 H COOEt J5 Me Gc Q61 H COOEt J5 OMe Gc CH.sub.2Q61H COOMe Me H G3 CH.sub.2Q61 H COOEt Me OMe Gc Q201 H COOMe Me H G3 Q201 H COOMe Me Me Gc Q201 H COOMe Me OMe Gc Q201 H COOMe Et H Gc Q201 H COOMe Et Me Gc Q201 H COOMe Et OMe G3 Q201 H COOMe J11 H Gc Q201 H COOMe J11 Me Gc Q201 H COOMe J11 OMeG3 Q201 H COOEt Me H Gc Q201 H COOEt Me Me G3 Q201 H COOEt Me OMe Gc Q201 H COOEt Et H Gc Q201 H COOEt Et Me G3 Q201 H COOEt Et OMe Gc Q201 H COOEt J12 H Gc Q201 H COOEt J12 Me Gc Q201 H COOEt J12 OMe Gc CH.sub.2Q201 H COOMe Me H G3 CH.sub.2Q201 H COOEt Me OMe Gc Q205 H COOMe Me H Gc Q205 H COOEt Me OMe Gc Q229 H COOMe Me H Gc Q229 H COOEt Me OMe G3 ______________________________________ TABLE 12 ______________________________________ ##STR34## A B D E W Gn ______________________________________ Q5 H COOMe Me O Gc CH.sub.2Q5 H COOMe Me O G3 Q5 H COOMe Et O Gc Q5 H COOMe Prn O Gc Q5 H COOMe CH.sub.2 CHCH.sub.2 O G3 Q5 HCOOMe OMe O Gc Q26 H COOMe Me O G3 Q26 H COOMe Et O Gc Q26 H COOMe OMe O Gc Q61 H COOMe Me O Gc CH.sub.2Q61 H COOMe Me O G3 Q61 H COOMe Et O Gc Q61 H COOMe Prn O Gc Q61 H COOMe CH.sub.2 CHCH.sub.2 O G3 Q61 H COOMe OMe O Gc Q5 H COOMe H S Gb CH.sub.2Q5 H COOMe H S G3 Q26 H COOMe H S Gc Q61 H COOMe H S Gc CH.sub.2Q61 H COOMe H S G3 Q5 H COOMe H NH Gb CH.sub.2Q5 H COOMe H NH G3 Q26 H COOMe H NH Gc Q61 H COOMe H NH Gc CH.sub.2Q61 H COOMe H NH G3 Q5 H COOMe H NOMe Gb CH.sub.2Q5 HCOOMe H NOMe G3 Q26 H COOMe H NOMe Gc Q61 H COOMe H NOMe Gc CH.sub.2Q61 H COOMe H NOMe G3 Q5 H COOEt Me O Gc CH.sub.2Q5 H COOEt Me O G3 Q5 H COOEt Et O Gc Q5 H COOEt Prn O Gc Q5 H COOEt CH.sub.2 CHCH.sub.2 O G3 Q5 H COOEt OMe O Gc Q26 HCOOEt Me O G3 Q26 H COOEt Et O Gc Q26 H COOEt OMe O Gc Q61 H COOEt Me O Gc CH.sub.2Q61 H COOEt Me O G3 Q61 H COOEt Et O Gc Q61 H COOEt Prn O Gc Q61 H COOEt CH.sub.2 CHCH.sub.2 O G3 Q61 H COOEt OMe O Gc Q5 H COOEt H S Gb CH.sub.2Q5 H COOEt HS G3 Q26 H COOEt H S Gc Q61 H COOEt H S Gc CH.sub.2Q61 H COOEt H S G3 Q5 H COOEt H NH Gb CH.sub.2Q5 H COOEt H NH G3 Q26 H COOEt H NH Gc Q61 H COOEt H NH Gc CH.sub.2Q61 H COOEt H NH G3 Q5 H COOEt H NOMe Gb CH.sub.2Q5 H COOEt H NOMe G3 Q26 HCOOEt H NOMe Gc Q61 H COOEt H NOMe Gc CH.sub.2Q61 H COOEt H NOMe G3 Q201 H COOMe Me O Gc CH.sub.2Q201 H COOMe Me O G3 Q201 H COOMe Et O Gc Q201 H COOMe Prn O Gc Q201 H COOMe CH.sub.2 CHCH.sub.2 O G3 Q201 H COOMe OMe O Gc Q205 H COOMe Me O G3 Q205 H COOMe Et O Gc Q205 H COOMe OMe O Gc Q201 H COOMe H S Gb CH.sub.2Q201 H COOMe H S G3 Q205 H COOMe H S Gc Q222 H COOMe H S G3 Q229 H COOMe H S G1 Q201 H COOMe H NH Gb CH.sub.2Q201 COOMe H NH G3 Q205 H COOMe H NH Gc Q222 H COOMe H NH Gc Q229 H COOMe H NH G3 Q201 H COOMe H NOMe Gb CH.sub.2 Q201 H COOMe H NOMe G3 Q205 H COOMe H NOMe Gc Q222 H COOMe H NOMe Gc Q229 H COOMe H NOMe G3 Q201 H COOEt Me O Gc CH.sub.2Q201 H COOEt Me O G3 Q201 H COOEt Et O Gc Q201 H COOEt Prn O Gc Q201H COOEt CH.sub.2 CHCH.sub.2 O Gc Q201 H COOEt OMe O Gc Q205 H COOEt Me O G3 Q205 H COOEt Et O G3 Q205 H COOEt OMe O Gc Q201 H COOEt H S Gb CH.sub.2Q201 H COOEt H S G3 Q205 H COOEt H S Gc Q222 H COOEt H S Gc Q229 H COOEt H S Gc Q201 H COOEt HNH Gb CH.sub.2Q201 H COOEt H NH G3 Q205 H COOEt H NH Gc Q222 H COOEt H NH Gc Q229 H COOEt H NH Gc Q201 H COOEt H NOMe Gb CH.sub.2Q201 H COOEt H NOMe G3 Q205 H COOEt H NOMe Gc Q222 H COOEt H NOMe Gc Q229 H COOEt H NOMe G3 ______________________________________ TABLE 13 ______________________________________ ##STR35## A B D W2 R22 Gn ______________________________________ Q5 H COOMe O Me Gc CH.sub.2 - Q5 H COOMe O Me G3 Q5 H COOMe O Et Gc Q5 H COOMe O Prn G3 Q26 H COOMe O Me Gc Q26 H COOMe OEt G3 Q61 H COOMe O Me Gc CH.sub.2 - Q61 H COOMe O Me G3 Q61 H COOMe O Et Gc Q61 H COOMe O Prn G3 Q158 H COOMe O Me Gc Q158 H COOMe O Et G3 Q5 H COOMe S Me Gc CH.sub.2 - Q5 H COOMe S Me G3 Q5 H COOMe S Et Gc Q5 H COOMe S Prn G3 Q26 H COOMe SMe Gc Q26 H COOMe S Et G3 Q61 H COOMe S Me Gc CH.sub.2 - Q61 H COOMe S Me G3 Q61 H COOMe S Et Gc Q61 H COOMe S Prn G3 Q158 H COOMe S Me Gc Q158 H COOMe S Et G3 Q5 H COOEt O Me Gc CH.sub.2 - Q5 H COOEt O Me G3 Q5 H COOEt O Et Gc Q5 H COOEt OPrn G3 Q26 H COOEt O Me Gc Q26 H COOEt O Et G3 Q61 H COOEt O Me Gc CH.sub.2 - Q61 H COOEt O Me G3 Q61 H COOEt O Et Gc Q61 H COOEt O Prn G3 Q158 H COOEt O Me Gc Q158 H COOEt O Et G3 Q5 H COOEt S Me Gc CH.sub.2 - Q5 H COOEt S Me G3 Q5 H COOEtS Et Gc Q5 H COOEt S Prn G3 Q26 H COOEt S Me Gc Q26 H COOEt S Et G3 Q61 H COOEt S Me Gc CH.sub.2 - Q61 H COOEt S Me G3 Q61 H COOEt S Et Gc Q61 H COOEt S Prn G3 Q158 H COOEt S Me Gc Q158 H COOEt S Et G3 Q201 H COOMe O Me Gc CH.sub.2 - Q201 HCOOMe O Me G.sub.3 Q201 H COOMe O Et Gc Q201 H COOMe O Prn Gc Q205 H COOMe O Me Gc Q205 H COOMe O Et Gc Q222 H COOMe O Me Gc Q222 H COOMe O Et G.sub.3 Q229 H COOMe O Me G.sub.3 Q229 H COOMe O Et Gc Q201 H COOMe S Me Gc CH.sub.2 - Q201 H COOMeS Me G.sub.3 Q201 H COOMe S Et Gc Q201 H COOMe S Prn Gc Q205 H COOMe S Me Gc Q205 H COOMe S Et Gc Q222 H COOMe S Me Gc Q222 H COOMe S Et G.sub.3 Q229 H COOMe S Me Gc Q229 H COOMe S Et G.sub.3 Q201 H COOEt O Me Gc CH.sub.2 - Q201 H COOEt O MeG.sub.3 Q201 H COOEt O Et Gc Q201 H COOEt O Prn Gc Q205 H COOEt O Me Gc Q205 H COOEt O Et Gc Q222 H COOEt O Me Gc Q222 H COOEt O Et G.sub.3 Q229 H COOEt O Me Gc Q229 H COOEt O Et G.sub..sub.3 Q201 H COOEt S Me Gc CH.sub.2 - Q201 H COOEt S MeG.sub.3 Q201 H COOEt S Et Gc Q201 H COOEt S Prn Gc Q205 H COOEt S Me Gc Q205 H COOEt S Et G.sub.3 Q222 H COOEt S Me Gc Q222 H COOEt S Et Gc Q229 H COOEt S Me G.sub.1 Q229 H COOEt S Et G.sub.1 ______________________________________ TABLE 14 ______________________________________ ##STR36## A B D Az Gn ______________________________________ Q5 H COOMe Imidazol-1-yl Gc Q5 H COOMe Pyrazol-1-yl Gc CH.sub.2 - Q5 H COOMe Imidazol-1-yl G.sub.1 CH.sub.2 - Q5 H COOMePyrazol-1-yl G.sub.1 Q26 H COOMe Imidazol-1-yl Gc Q26 H COOMe Pyrazol-1-yl Gc Q61 H COOMe Imidazol-1-yl Gc Q61 H COOMe Pyrazol-1-yl Gc CH.sub.2 - Q61 H COOMe Imidazol-1-yl G.sub.3 CH.sub.2 - Q61 H COOMe Pyrazol-1-yl G.sub.3 Q5 H COOEtImidazol-1-yl Gc Q5 H COOEt Pyrazol-1-yl Gc CH.sub.2 - Q5 H COOEt Imidazol-1-yl G.sub.3 CH.sub.2 - Q5 H COOEt Pyrazol-1-yl G.sub.3 Q26 H COOEt Imidazol-1-yl Gc Q26 H COOEt Pyrazol-1-yl Gc Q61 H COOEt Imidazol-1-yl Gc Q61 H COOEtPyrazol-1-yl Gc CH.sub.2 - Q61 H COOEt Imidazol-1-yl G.sub.3 CH.sub.2 - Q61 H COOEt Pyrazol-1-yl G.sub.3 Q201 H COOMe Imidazol-1-yl Gc Q201 H COOMe Pyrazol-1-yl Gc CH.sub.2 - Q201 H COOMe Imidazol-1-yl G.sub.1 CH.sub.2 - Q201 H COOMePyrazol-1-yl G.sub.1 Q205 H COOMe Imidazol-1-yl Gc Q205 H COOMe Pyrazol-1-yl Gc Q222 H COOMe Imidazol-1-yl Gc Q222 H COOMe Pyrazol-1-yl Gc Q229 H COOMe Imidazol-1-yl G.sub.3 Q229 H COOMe Pyrazol-1-yl G.sub.3 Q201 H COOEt Imidazol-1-yl Gc Q201 H COOEt Pyrazol-1-yl Gc CH.sub.2 - Q201 H COOEt Imidazol-1-yl G.sub.3 CH.sub.2 - Q201 H COOEt Pyrazol-1-yl G.sub.3 Q205 H COOEt Imidazol-1-yl Gc Q205 H COOEt Pyrazol-1-yl Gc Q222 H COOEt Imidazol-1-yl Gc Q222 H COOEt Pyrazol-1-yl Gc Q229 H COOEt Imidazol-1-yl G.sub.3 Q229 H COOEt Pyrazol-1-yl G.sub.3 ______________________________________ TABLE 15 ______________________________________ ##STR37## A B D J R.sup.23 Gn ______________________________________ Q5 H COOMe Me H G3 Q5 H COOMe Me Me Gc Q5 H COOMe Me OMe Gc Q5 H COOMe Et H Gc Q5 H COOMe Et Me Gc Q5 H COOMe Et OMe G3 Q5 H COOMe J6 H Gc Q5 H COOMe J6 Me Gc Q5 H COOMe J6 OMe G3 Q5 H COOEt Me H Gc Q5 H COOEt Me Me G3 Q5 H COOEt Me OMe Gc Q5 H COOEt Et H Gc Q5 H COOEt Et Me G3 Q5 H COOEt Et OMe Gc Q5 H COOEt J7 H Gc Q5 H COOEt J7 Me Gc Q5 H COOEt J7 OMe Gc CH.sub.2 - Q5 H COOMe Me H G3 CH.sub.2 - Q5 H COOEt Me OMe Gc Q26 H COOMe Me H Gc Q26 H COOEt Me OMe Gc Q61 H COOMe Me H G3 Q61 H COOMe Me Me Gc Q61 H COOMe Me OMe Gc Q61 H COOMe Et H Gc Q61 H COOMe Et Me Gc Q61 H COOMe Et OMe G3 Q61 H COOMeJ8 H Gc Q61 H COOMe J8 Me Gc Q61 H COOMe J8 OMe G3 Q61 H COOEt Me H Gc Q61 H COOEt Me Me G3 Q61 H COOEt Me OMe Gc Q61 H COOEt Et H Gc Q61 H COOEt Et Me G3 Q61 H COOEt Et OMe Gc Q61 H COOEt J9 H Gc Q61 H COOEt J9 Me Gc Q61 H COOEt J9 OMe Gc CH.sub.2 - Q61 H COOMe Me H G3 CH.sub.2 - Q61 H COOEt Me OMe Gc Q201 H COOMe Me H G.sub.3 Q201 H COOMe Me Me Gc Q201 H COOMe Me OMe Gc Q201 H COOMe Et H Gc Q201 H COOMe Et Me Gc Q201 H COOMe Et OMe G.sub.3 Q201 H COOMe J13 H Gc Q201 H COOMeJ13 Me Gc Q201 H COOMe J13 OMe G.sub.3 Q201 H COOEt Me H Gc Q201 H COOEt Me Me G.sub.3 Q201 H COOEt Me OMe Gc Q201 H COOEt Et H Gc Q201 H COOEt Et Me G.sub.3 Q201 H COOEt Et OMe Gc Q201 H COOEt J14 H Gc Q201 H COOEt J14 Me Gc Q201 H COOEt J14OMe Gc CH.sub.2 - Q201 H COOMe Me H G.sub.3 CH.sub.2 - Q201 H COOEt Me OMe Gc Q205 H COOMe Me H Gc Q205 H COOEt Me OMe Gc Q229 H COOMe Me H Gc Q229 H COOEt Me OMe G.sub.3 ______________________________________ In application of the compounds of this invention as herbicides, they can be applied by mixing with suitable carriers such as solid carriers, including for example clay, talc, bentonite, diatomaceous earth and others, or liquid carriers,including for example water, alcohols (methanol, ethanol and the like), aromatic hydrocarbons (benzene, toluene, xylene and the like), chlorinated hydrocarbons, ethers, ketones, esters (ethyl acetate etc.), acid amides (dimethylformamide etc.) andothers. They can be provided for practical use with addition of any desired additive selected from an emulsifier, a dispersing agent, a suspending agent, a penetrating agent, a spreader and a stabilizer and in any desired form such as a solubleconcentrate, an emulsifiable concentrate, a wettable powder, a dust, a granule, a flowable, etc. In the following, there are shown examples of formulations of herbicides containing the compounds of this invention as active ingredients, but they are not limitative of this invention. In the exemplary formulations shown below, "parts" means"parts by weight". ______________________________________ Exemplary Formulation 1: Wettable powder ______________________________________ Compound No. 11 of this invention 20 parts Zeeklite A 76 parts (kaolin type clay; trade name; produced by Zeeklite KogyoCo., Ltd.) Solpol 5039 2 parts (mixture of nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) Carplex (anticaking agent) 2 parts (white carbon; trade name, produced by Shionogi Seiyaku Co., Ltd.) ______________________________________ The above components are mixed and pulverized homogeneously to prepare a wettable powder. ______________________________________ Exemplary Formulation 2: Wettable powder ______________________________________ Compound No. 6 of this invention 40 parts Zeeklite A 54 parts (kaolin type clay; trade name; produced by Zeeklite KogyoCo., Ltd.) Solpol 5039 2 parts (mixture of nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) Carplex (anticaking agent) 4 parts (white carbon; trade name, produced by Shionogi Seiyaku Co., Ltd.) ______________________________________ The above components are mixed and pulverized homogeneously to prepare a wettable powder. ______________________________________ Exemplary Formulation 3: Emulsifiable concentrate ______________________________________ Compound No. 3 of this invention 5 parts Xylene 75 parts Dimethylformamide 15 parts Solpol 2680 5 parts (mixtureof nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) ______________________________________ The above components are homogeneously mixed to prepare an emulsifiable concentrate. In use, the above emulsifiable concentrate is diluted 10 to 10,000 times and sprayed in an amount of 0.005 to 10 kg per hectare in terms of the activeingredient. ______________________________________ Exemplary Formulation 4: Flowable ______________________________________ Compound No. 11 of this invention 25 parts Agrisol S-710 10 parts (nonionic surfactant; trade name; produced by Kao Co., Ltd.) Runox 1000C 0.5 part (anionic surfactant; trade name; produced by Toho Kagaku Co., Ltd.) 1% Rhodopol water 20 parts (thickener; trade name, produced by Rhone-Poulenc Co., Ltd.) Water 44.5 parts ______________________________________ The above components are mixed homogeneously to provide a flowable agent. ______________________________________ Exemplary Formulation 5: Flowable ______________________________________ Compound No. 9 of this invention 40 parts Agrisol S-710 10 parts (nonionic surfactant; trade name; produced by Kao Co., Ltd.) Runox 1000C 0.5 part (anionic surfactant; trade name; produced by Toho Kagaku Co., Ltd.) 1% Rhodopol water 20 parts (thickener; trade name, produced by Rhone-Poulenc Co., Ltd.) Water 29.5 parts ______________________________________ The above components are mixed homogeneously to provide a flowable agent. ______________________________________ Exemplary Formulation 6: Granule ______________________________________ Compound No. 8 of this invention 1 part Bentonite 55 parts Talc 44 parts ______________________________________ The above components are mixed and pulverized homogeneously, then a small amount of water is added and the whole is stirred, kneaded and granulated by excluding granulator, then dried to prepare a granule. ______________________________________ Exemplary Formulation 7: Wettable powder ______________________________________ Compound No. 24 of this invention 20 parts Zeeklite A 76 parts (kaolin type clay; trade name; produced by Zeeklite KogyoCo., Ltd.) Solpol 5039 2 parts (mixture of nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) Carplex (anticaking agent) 2 parts (white carbon; trade name, produced by Shionogi Seiyaku Co., Ltd.) ______________________________________ The above components are mixed and pulverized homogeneously to prepare a wettable powder. ______________________________________ Exemplary Formulation 8: Wettable powder ______________________________________ Compound No. 21 of this invention 40 parts Zeeklite A 54 parts (kaolin type clay; trade name; produced by Zeeklite KogyoCo., Ltd.) Solpol 5039 2 parts (mixture of nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) Carplex (anticaking agent) 4 parts (white carbon; trade name, produced by Shionogi Seiyaku Co., Ltd.) ______________________________________ The above components are mixed and pulverized homogeneously to prepare a wettable powder. ______________________________________ Exemplary Formulation 9: Emulsifiable concentrate ______________________________________ Compound No. 22 of this invention 5 parts Xylene 75 parts Dimethylformamide 15 parts Solpol 2680 5 parts (mixture of nonionic surfactant and anionic surfac- tant; trade name; produced by Toho Kagaku Co., Ltd.) ______________________________________ The above components are homogeneously mixed to prepare an emulsifiable concentrate. In use, the above emulsifiable concentrate is diluted 10 to 10,000 times and sprayed in an amount of 0.005 to 10 kg per hectare in terms of the activeingredient. ______________________________________ Exemplary Formulation 10: Flowable ______________________________________ Compound No. 24 of this invention 25 parts Agrisol S-710 10 parts (nonionic surfactant; trade name; produced by Kao Co., Ltd.) Runox 1000C 0.5 part (anionic surfactant; trade name; produced by Toho Kagaku Co., Ltd.) 1% Rhodopol water 20 parts (thickener; trade name, produced by Rhone-Poulenc Co., Ltd.) Water 44.5 parts ______________________________________ The above components are mixed homogeneously to provide a flowable agent. ______________________________________ Exemplary Formulation 11: Flowable ______________________________________ Compound No. 21 of this invention 40 parts Agrisol S-710 10 parts (nonionic surfactant; trade name; produced by Kao Co., Ltd.) Runox 1000C 0.5 part (anionic surfactant; trade name; produced by Toho Kagaku Co., Ltd.) 1% Rhodopol water 20 parts (thickener; trade name, produced by Rhone-Poulenc Co., Ltd.) Water 29.5 parts ______________________________________ The above components are mixed homogeneously to provide a flowable agent. ______________________________________ Exemplary Formulation 12: Granule ______________________________________ Compound No. 23 of this invention 1 part Bentonite 55 parts Talc 44 parts ______________________________________ The above components are mixed and pulverized homogeneously, then a small amount of water is added and the whole is stirred, kneaded and granulated by excluding granulator, then dried to prepare a granule. If desired, the compound of this invention may be applied as a mixture with other kinds of herbicides, various insecticides, sterilizers or adjuvants during preparation or before spraying. Such other kinds of herbicides as mentioned above include compounds as described in Farm Chemicals Handbook (1986). The compounds of this invention can also be applied not only to the agricultural and horticultural fields such as farm fields, paddy fields, fruit gardens and the like, but to the non-agricultural fields such as athletic grounds, vacant lands,belts along railroads and others in order to prevent and eliminate various weeds. The amounts of the herbicide to be applied, which may differ depending on the scenes to be applied, the time of application, the application method, the kinds of theobjective grasses and the crops harvested, may generally range suitably from about 0.005 to 10 kg per hectare in terms of the active ingredient. The following test examples are set forth for illustrating specifically the effectiveness of the compounds of this invention as herbicides. TEST EXAMPLE 1 Herbicidal effect test by soil treatment In a plastic box of 15 cm length, 22 cm width and 6 cm depth, there was placed a sterilized deluvium soil, and seeds of (A) barnyardgrass (Echinochloa crusgalli), (B) large crabgrass (Digitaria adscendens), (C) annual sedge (Cyperus microiria),(D) black nightshade (Solanum nigrum L.), (E) hairly galinosoga (Galinosoga ciliata), (F) yellows cress (Rorippa atrovirens), (G) rice (Oryza sativa), (H) corn (Zea mays), (I) wheat (Triticum vulgare), (J) soybean (Glysine max), (K) cotton (Gossypiumspp) and (L) sugar beet (Beta vulgaris) were sown mixedly. After covering the seeds with soil to about 1.5 cm, herbicides were sprayed evenly on the soil surface respectively such that a predetermined proportion of the active ingredient may be applied. In spraying, the wettable powder as shown in the foregoing exemplary formulations was diluted with water and sprayed over the entire surface by means of a small sprayer. Four weeks after spraying, the herbicidal effect on crops and each of theweeds were examined according to the judgment criteria shown below. Provided that, in the following Table, a mark "-" was shown in the column of activity when beet was omitted from the crops to be tested. The results are shown in Table 16. Some of the compounds of this invention show the selectivity on certain crops. ______________________________________ Judgment criteria: ______________________________________ 5 . . . Growth control rates of more than 90% (almost completely withered) 4 . . . Growth control rates of 70 to 90% 3 . . . Growth control ratesof 40 to 70% 2 . . . Growth control rates of 20 to 40% 1 . . . Growth control rates of 5 to 20% 0 . . . Growth control rates of less than 5% (substantially no effect) ______________________________________ The above growth control rates are determined by measuring the top fresh weights of the treated plants and those of the non-treated plants, and calculated from the following formula: ##EQU1## TABLE 16 __________________________________________________________________________ Amount of ac- tive ingredi- Compound ent applied No. kg/ha (A) (B) (C) (D) (E) (F) (G) (H) (I) (J) (K) (L) __________________________________________________________________________ 3 0.32 5 4 5 4 4 5 5 5 5 5 0 -- 6 0.32 5 5 5 5 5 5 5 5 5 5 0 -- 9 0.16 5 5 5 5 5 5 5 5 5 5 0 -- 0.32 5 5 5 5 5 5 5 5 5 5 0 -- 11 0.08 5 5 5 5 5 5 5 5 5 5 5 0 0.16 5 5 5 5 5 55 5 5 5 5 0 13 0.16 5 5 5 5 5 5 5 5 5 5 5 0 16 0.08 5 3 5 5 5 5 5 5 3 3 0 0 0.16 5 4 5 5 5 5 5 5 4 4 1 0 19 0.04 4 3 5 5 5 5 5 5 5 5 5 -- 0.08 5 4 5 5 5 5 5 5 5 5 5 -- 0.16 5 5 5 5 5 5 5 5 5 5 5 -- 21 0.04 4 4 4 4 5 5 5 4 0 4 0 -- 0.08 5 5 5 5 55 5 5 1 5 0 -- 0.16 5 5 5 5 5 5 5 5 2 5 1 -- 24 0.02 5 4 5 5 5 5 5 5 5 5 0 -- 0.04 5 5 5 5 5 5 5 5 5 5 0 -- 0.08 5 5 5 5 5 5 5 5 5 5 0 -- __________________________________________________________________________ (A) barnyardgrass (Echinochloacrusgalli), (B) large crabgrass (Digitaria adscendens), (C) annual sedge (Cyperus microiria), (D) black nightshade (Solanum nigrum L.), (E) hairly galinosoga (Galinosoga ciliata), (F) yellows cress (Rorippa atrovirens), (G) rice (Oryza sativa), (H) corn (Zea mays), (I) wheat (Triticum vulgare), (J) soybean (Glysine max), (K) cotton (Gossypium spp), (L) sugar beet (Beta vulgaris). TEST EXAMPLE 2 Herbicidal effect test by foliage treatment In a plastic box of 15 cm length, 22 cm width and 6 cm depth, there was placed a sterilized deluvium soil, and seeds of (A) barnyardgrass (Echinochloa crusgalli), (B) large crabgrass (Digitaria adscendens), (C) annual sedge (Cyperus microiria),(D) black nightshade (Solanum nigrum L.), (E) hairly galinosoga (Galinosoga ciliata), (F) yellows cress (Rorippa atrovirens), (G) rice (Oryza sativa), (H) corn (Zea mays), (I) wheat (Triticum vulgare), (J) soybean (Glysine max), (K) cotton (Gossypiumspp) and (L) sugar beet (Beta vulgaris) were sown in spots. After covering the seeds with soil to about 1.5 cm, herbicides were sprayed evenly on the soil surface such that a predetermined proportion of the active ingredient may be applied. In spraying, the wettable powder as shown in the foregoing exemplary formulations was diluted with water and sprayed over the entire surface of the foliage portions of each crop and weed by means of a small sprayer. Four weeks after spraying,the herbicidal effect on crops etc. and each of the weeds were examined according to the judgment criteria shown in Test Example 1. The results are shown in Table 17. TABLE 17 __________________________________________________________________________ Amount of ac- tive ingredi- Compound ent applied No. kg/ha (A) (B) (C) (D) (E) (F) (G) (H) (I) (J) (K) (L) __________________________________________________________________________ 3 0.08 5 2 5 5 5 5 5 5 5 5 0 5 0.16 5 3 5 5 5 5 5 5 5 5 1 5 5 0.32 5 5 5 5 5 5 5 5 5 5 5 -- 6 0.04 5 1 4 5 5 5 5 5 0 5 5 5 0.08 5 2 5 5 5 5 5 5 1 5 5 5 0.16 5 3 5 5 5 5 5 5 25 5 5 8 0.08 4 1 5 5 5 5 5 4 0 5 4 5 0.16 5 2 5 5 5 5 5 5 0 5 5 5 9 0.04 5 3 4 5 5 5 5 5 4 5 5 5 0.08 5 4 5 5 5 5 5 5 5 5 5 5 0.16 5 5 5 5 5 5 5 5 5 5 5 5 11 0.04 5 4 5 5 5 5 5 5 5 5 5 0 0.08 5 5 5 5 5 5 5 5 5 5 5 0 0.16 5 5 5 5 5 5 5 5 5 5 5 0 13 0.16 5 5 5 5 5 5 5 5 5 5 5 0 16 0.08 5 4 5 5 5 5 5 5 5 5 5 0 0.16 5 5 5 5 5 5 5 5 5 5 5 0 19 0.04 5 4 5 5 5 5 5 5 5 5 5 5 0.08 5 5 5 5 5 5 5 5 5 5 5 5 0.16 5 5 5 5 5 5 5 5 5 5 5 5 21 0.02 3 2 5 5 5 5 5 5 4 5 4 5 0.04 4 3 5 5 5 5 5 5 5 5 5 5 0.08 5 4 5 5 5 5 5 5 5 5 5 5 24 0.01 5 4 5 5 5 5 5 5 4 5 4 5 0.02 5 5 5 5 5 5 5 5 5 5 5 5 0.04 5 5 5 5 5 5 5 5 5 5 5 5 __________________________________________________________________________ (A) barnyardgrass (Echinochloa crusgalli), (B) largecrabgrass (Digitaria adscendens), (C) annual sedge (Cyperus microiria), (D) black nightshade (Solanum nigrum L.), (E) hairly galinosoga (Galinosoga ciliata), (F) yellows cress (Rorippa atrovirens), (G) rice (Oryza sativa), (H) corn (Zea mays), (I)wheat (Triticum vulgare), (J) soybean (Glysine max), (K) cotton (Gossypium spp), (L) sugar beet (Beta vulgaris). * * * * *       Recently Added Patents Low glare, high print gloss printing paper Light scanning apparatus, image forming apparatus equipped with such light scanning apparatus, and control method or image forming method for such image forming apparatus Imaging using media carriage coupled to a lid Method for computing patient radiation dose in computed tomography Apparatus and method for performing MD5 digesting Process for the identification of objects Shroud for axial flow fan   Randomly Featured Patents Motion estimation method by employing a stochastic sampling technique Sanitary head covering and method of manufacture Method for the production of impact polystyrene Vehicle reaction timer Apparatus having printed circuit pattern for suppressing radio interference Treatment of stroke or in anticipation of the occurrence of brain ischemia Voltage-controlled oscillator and communication device Method and apparatus for cleaning a heater bellow in a chemical vapor deposition chamber Tissue removal methods and apparatus Carbonized product used for production of activated carbon for electrode of electric double-layer capacitor © 2006. 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